ABO c.99-288T>C

Variant ID: 9-136137065-A-G

NM_020469.2(ABO):c.99-288T>C

This variant was identified in 53 publications

View GRCh38 version.




Publications:


Assessing the potential of polygenic scores to strengthen medical risk prediction models of COVID-19.

Plos One
Córdova-Palomera, Aldo A; Siffel, Csaba C; DeBoever, Chris C; Wong, Emily E; Diogo, Dorothée D; Szalma, Sandor S
Publication Date: 2023

Variant appearance in text: rs687621
PubMed Link: 37235597
Variant Present in the following documents:
  • Main text
  • pone.0285991.pdf
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Association of Inherited Genetic Factors With Drug-Induced Hepatic Damage Among Children With Acute Lymphoblastic Leukemia.

Jama Network Open
Yang, Wenjian W; Karol, Seth E SE; Hoshitsuki, Keito K; Lee, Shawn S; Larsen, Eric C EC; Winick, Naomi N; Carroll, William L WL; Loh, Mignon L ML; Raetz, Elizabeth A EA; Hunger, Stephen P SP; Winter, Stuart S SS; Dunsmore, Kimberly P KP; Devidas, Meenakshi M; Relling, Mary V MV; Yang, Jun J JJ
Publication Date: 2022-12-01

Variant appearance in text: rs687621
PubMed Link: 36580335
Variant Present in the following documents:
  • jamanetwopen-e2248803-s001.pdf
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Genotype imputation and polygenic score estimation in northwestern Russian population.

Plos One
Kolosov, Nikita N; Rezapova, Valeriia V; Rotar, Oxana O; Loboda, Alexander A; Freylikhman, Olga O; Melnik, Olesya O; Sergushichev, Alexey A; Stevens, Christine C; Voortman, Trudy T; Kostareva, Anna A; Konradi, Alexandra A; Daly, Mark J MJ; Artomov, Mykyta M
Publication Date: 2022

Variant appearance in text: rs687621
PubMed Link: 35763490
Variant Present in the following documents:
  • pone.0269434.s001.pdf
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The Genetic Risk for COVID-19 Severity Is Associated With Defective Immune Responses.

Frontiers In Immunology
Kuijpers, Yunus Y; Chu, Xiaojing X; Jaeger, Martin M; Moorlag, Simone J C F M SJCFM; Koeken, Valerie A C M VACM; Zhang, Bowen B; de Nooijer, Aline A; Grondman, Inge I; Gupta, Manoj Kumar MK; Janssen, Nico N; Mourits, Vera P VP; de Bree, L Charlotte J LCJ; de Mast, Quirijn Q; van de Veerdonk, Frank L FL; Joosten, Leo A B LAB; Li, Yang Y; Netea, Mihai G MG; Xu, Cheng-Jian CJ
Publication Date: 2022

Variant appearance in text: rs687621
PubMed Link: 35634344
Variant Present in the following documents:
  • Main text
  • fimmu-13-859387.pdf
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ABO O blood group as a risk factor for platelet reactivity in heparin-induced thrombocytopenia.

Blood
Karnes, Jason H JH; Rollin, Jerome J; Giles, Jason B JB; Martinez, Kiana L KL; Steiner, Heidi E HE; Shaffer, Christian M CM; Momozawa, Yukihide Y; Inai, Chihiro C; Bombin, Andrei A; Shi, Mingjian M; Mosley, Jonathan D JD; Stanaway, Ian I; Selleng, Kathleen K; Thiele, Thomas T; Mushiroda, Taisei T; Pouplard, Claire C; Heddle, Nancy M NM; Kubo, Michiaki M; Phillips, Elizabeth J EJ; Warkentin, Theodore E TE; Gruel, Yves Y; Greinacher, Andreas A; Roden, Dan M DM
Publication Date: 2022-07-21

Variant appearance in text: rs687621
PubMed Link: 35377938
Variant Present in the following documents:
  • bloodBLD2021014240-suppl1.pdf
  • 10.1182-2021014240_bloodbld2021014240-suppl1.pdf
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Integrative genetic and immune cell analysis of plasma proteins in healthy donors identifies novel associations involving primary immune deficiency genes.

Genome Medicine
Caron, Barthelemy B; Patin, Etienne E; Rotival, Maxime M; Charbit, Bruno B; Albert, Matthew L ML; Quintana-Murci, Lluis L; Duffy, Darragh D; Rausell, Antonio A; ,
Publication Date: 2022-03-09

Variant appearance in text: rs687621
PubMed Link: 35264221
Variant Present in the following documents:
  • Main text
  • 13073_2022_Article_1032.pdf
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Insilico Functional Analysis of Genome-Wide Dataset From 17,000 Individuals Identifies Candidate Malaria Resistance Genes Enriched in Malaria Pathogenic Pathways.

Frontiers In Genetics
Damena, Delesa D; Agamah, Francis E FE; Kimathi, Peter O PO; Kabongo, Ntumba E NE; Girma, Hundaol H; Choga, Wonderful T WT; Golassa, Lemu L; Chimusa, Emile R ER
Publication Date: 2021

Variant appearance in text: rs687621
PubMed Link: 34868193
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification and replication of novel genetic variants of ABO gene to reduce the incidence of diseases and promote longevity by modulating lipid homeostasis.

Aging
Ni, Xiaolin X; Bai, Chen C; Nie, Chao C; Qi, Liping L; Liu, Yifang Y; Yuan, Huiping H; Zhu, Xiaoquan X; Sun, Liang L; Zhou, Qi Q; Li, Yan Y; Zhen, Hefu H; Su, Huabing H; Li, Rongqiao R; Lan, Rushu R; Pang, Guofang G; Lv, Yuan Y; Zhang, Wei W; Yang, Fan F; Yao, Yao Y; Chen, Chen C; Wang, Zhaoping Z; Gao, Danni D; Zhang, Nan N; Zhang, Shenqi S; Zhang, Li L; Wu, Zhu Z; Hu, Caiyou C; Zeng, Yi Y; Yang, Ze Z
Publication Date: 2021-11-22

Variant appearance in text: rs687621
PubMed Link: 34812738
Variant Present in the following documents:
  • Main text
  • aging-13-203700.pdf
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Identification and replication of novel genetic variants of ABO gene to reduce the incidence of diseases and promote longevity by modulating lipid homeostasis.

Aging
Ni, Xiaolin X; Bai, Chen C; Nie, Chao C; Qi, Liping L; Liu, Yifang Y; Yuan, Huiping H; Zhu, Xiaoquan X; Sun, Liang L; Zhou, Qi Q; Li, Yan Y; Zhen, Hefu H; Su, Huabing H; Li, Rongqiao R; Lan, Rushu R; Pang, Guofang G; Lv, Yuan Y; Zhang, Wei W; Yang, Fan F; Yao, Yao Y; Chen, Chen C; Wang, Zhaoping Z; Gao, Danni D; Zhang, Nan N; Zhang, Shenqi S; Zhang, Li L; Wu, Zhu Z; Hu, Caiyou C; Zeng, Yi Y; Yang, Ze Z
Publication Date: 2021-11-22

Variant appearance in text: rs687621
PubMed Link: 34812738
Variant Present in the following documents:
  • Main text
  • aging-13-203700.pdf
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An assessment of the effect of the genotype on postoperative venous thromboembolism risk in 140,831 surgical patients.

Annals Of Medicine And Surgery (2012)
A Christensen, Mathias M; Bonde, Alexander A; Sillesen, Martin M
Publication Date: 2021-11

Variant appearance in text: rs687621
PubMed Link: 34777790
Variant Present in the following documents:
  • Main text
  • main.pdf
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Effects of Insomnia on Peptic Ulcer Disease Using Mendelian Randomization.

Oxidative Medicine And Cellular Longevity
Zha, Ling-Feng LF; Dong, Jiang-Tao JT; Wang, Jing-Lin JL; Chen, Qian-Wen QW; Wu, Jian-Fei JF; Zhou, Ying-Chao YC; Nie, Shao-Fang SF; Tu, Xin X
Publication Date: 2021

Variant appearance in text: rs687621
PubMed Link: 34616502
Variant Present in the following documents:
  • Main text
  • OMCL2021-2216314.pdf
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Genetically Predicted Insomnia in Relation to 14 Cardiovascular Conditions and 17 Cardiometabolic Risk Factors: A Mendelian Randomization Study.

Journal Of The American Heart Association
Liu, Xinhui X; Li, Chuanbao C; Sun, Xiaoru X; Yu, Yuanyuan Y; Si, Shucheng S; Hou, Lei L; Yan, Ran R; Yu, Yifan Y; Li, Mingzhuo M; Li, Hongkai H; Xue, Fuzhong F
Publication Date: 2021-08-03

Variant appearance in text: rs687621
PubMed Link: 34315237
Variant Present in the following documents:
  • JAH3-10-e020187-s001.pdf
  • JAH3-10-e020187.pdf
View BVdb publication page



Circulating white blood cells and lung function impairment: the observational studies and Mendelian randomization analysis.

Annals Of Medicine
Wu, Xiulong X; Wang, Chenming C; Li, Hang H; Meng, Hua H; Jie, Jiali J; Fu, Ming M; Bai, Yansen Y; Li, Guyanan G; Wei, Wei W; Feng, Yue Y; Li, Mengying M; Guan, Xin X; He, Meian M; Zhang, Xiaomin X; Guo, Huan H
Publication Date: 2021-12

Variant appearance in text: rs687621
PubMed Link: 34259107
Variant Present in the following documents:
  • IANN_A_1948603_SM3508.pdf
View BVdb publication page



Associations between Genetically Predicted Circulating Protein Concentrations and Endometrial Cancer Risk.

Cancers
Zhu, Jingjing J; O'Mara, Tracy A TA; Liu, Duo D; Setiawan, Veronica Wendy VW; Glubb, Dylan D; Spurdle, Amanda B AB; Fasching, Peter A PA; Lambrechts, Diether D; Buchanan, Daniel D; Kho, Pik Fang PF; Cook, Linda S LS; Friedenreich, Christine C; Lacey, James V JV; Chen, Chu C; Wentzensen, Nicolas N; De Vivo, Immaculata I; Sun, Yan Y; Long, Jirong J; Du, Mengmeng M; Shu, Xiao-Ou XO; Zheng, Wei W; Wu, Lang L; Yu, Herbert H
Publication Date: 2021-04-26

Variant appearance in text: rs687621
PubMed Link: 33925895
Variant Present in the following documents:
  • Main text
View BVdb publication page



GWAS of peptic ulcer disease implicates Helicobacter pylori infection, other gastrointestinal disorders and depression.

Nature Communications
Wu, Yeda Y; Murray, Graham K GK; Byrne, Enda M EM; Sidorenko, Julia J; Visscher, Peter M PM; Wray, Naomi R NR
Publication Date: 2021-02-19

Variant appearance in text: rs687621
PubMed Link: 33608531
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genome-wide association study of serum liver enzymes implicates diverse metabolic and liver pathology.

Nature Communications
Chen, Vincent L VL; Du, Xiaomeng X; Chen, Yanhua Y; Kuppa, Annapurna A; Handelman, Samuel K SK; Vohnoutka, Rishel B RB; Peyser, Patricia A PA; Palmer, Nicholette D ND; Bielak, Lawrence F LF; Halligan, Brian B; Speliotes, Elizabeth K EK
Publication Date: 2021-02-05

Variant appearance in text: rs687621
PubMed Link: 33547301
Variant Present in the following documents:
  • 41467_2020_20870_MOESM1_ESM.pdf
View BVdb publication page



Association between ABO haplotypes and the risk of venous thrombosis: impact on disease risk estimation.

Blood
Goumidi, Louisa L; Thibord, Florian F; Wiggins, Kerri L KL; Li-Gao, Ruifang R; Brown, Mickael R MR; van Hylckama Vlieg, Astrid A; Souto, Joan-Carles JC; Soria, José-Manuel JM; Ibrahim-Kosta, Manal M; Saut, Noémie N; Daian, Delphine D; Olaso, Robert R; Amouyel, Philippe P; Debette, Stéphanie S; Boland, Anne A; Bailly, Pascal P; Morrison, Alanna C AC; Mook-Kanamori, Denis O DO; Deleuze, Jean-François JF; Johnson, Andrew A; de Vries, Paul S PS; Sabater-Lleal, Maria M; Chiaroni, Jacques J; Smith, Nicholas L NL; Rosendaal, Frits R FR; Chasman, Daniel I DI; Trégouët, David-Alexandre DA; Morange, Pierre-Emmanuel PE
Publication Date: 2021-04-29

Variant appearance in text: rs687621
PubMed Link: 33512453
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients.

Th Open : Companion Journal To Thrombosis And Haemostasis
Manderstedt, Eric E; Lind-Halldén, Christina C; Lethagen, Stefan S; Halldén, Christer C
Publication Date: 2020-10

Variant appearance in text: rs687621
PubMed Link: 33145474
Variant Present in the following documents:
  • Main text
View BVdb publication page



Gene Variants Associated With Venous Thrombosis: A Replication Study in a Brazilian Multicentre Study.

Clinical And Applied Thrombosis/Hemostasis : Official Journal Of The International Academy Of Clinical And Applied Thrombosis/Hemostasis
Romano, Anna Virgínia Calazans AVC; Barnabé, Aline A; Gadelha, Telma Barbosa TB; Guerra, João Carlos de Campos JCC; Secolin, Rodrigo R; Orsi, Fernanda Loureiro de Andrade FLA; Campanate, Gizele de Castro Sousa GCS; Wolosker, Nelson N; Annichino-Bizzacchi, Joyce Maria JM
Publication Date: 2020

Variant appearance in text: rs687621
PubMed Link: 33119405
Variant Present in the following documents:
  • Main text
  • 10.1177_1076029620962225.pdf
View BVdb publication page



Mendelian Randomization Analysis of Hemostatic Factors and Their Contribution to Peripheral Artery Disease-Brief Report.

Arteriosclerosis, Thrombosis, And Vascular Biology
Small, Aeron M AM; Huffman, Jennifer E JE; Klarin, Derek D; Sabater-Lleal, Maria M; Lynch, Julie A JA; Assimes, Themistocles L TL; Sun, Yan V YV; Miller, Donald D; Freiberg, Matthew S MS; Morrison, Alanna C AC; Rader, Daniel J DJ; Wilson, Peter W F PWF; Cho, Kelly K; Tsao, Philip S PS; Chang, Kyong-Mi KM; Smith, Nicholas L NL; O'Donnell, Christopher J CJ; de Vries, Paul S PS; Damrauer, Scott M SM; ,
Publication Date: 2021-01

Variant appearance in text: rs687621
PubMed Link: 32847391
Variant Present in the following documents:
  • Main text
View BVdb publication page



Associations between Genetically Predicted Blood Protein Biomarkers and Pancreatic Cancer Risk.

Cancer Epidemiology, Biomarkers & Prevention : A Publication Of The American Association For Cancer Research, Cosponsored By The American Society Of Preventive Oncology
Zhu, Jingjing J; Shu, Xiang X; Guo, Xingyi X; Liu, Duo D; Bao, Jiandong J; Milne, Roger L RL; Giles, Graham G GG; Wu, Chong C; Du, Mengmeng M; White, Emily E; Risch, Harvey A HA; Malats, Nuria N; Duell, Eric J EJ; Goodman, Phyllis J PJ; Li, Donghui D; Bracci, Paige P; Katzke, Verena V; Neale, Rachel E RE; Gallinger, Steven S; Van Den Eeden, Stephen K SK; Arslan, Alan A AA; Canzian, Federico F; Kooperberg, Charles C; Beane Freeman, Laura E LE; Scelo, Ghislaine G; Visvanathan, Kala K; Haiman, Christopher A CA; Le Marchand, Loïc L; Yu, Herbert H; Petersen, Gloria M GM; Stolzenberg-Solomon, Rachael R; Klein, Alison P AP; Cai, Qiuyin Q; Long, Jirong J; Shu, Xiao-Ou XO; Zheng, Wei W; Wu, Lang L
Publication Date: 2020-07

Variant appearance in text: rs687621
PubMed Link: 32439797
Variant Present in the following documents:
  • Main text
View BVdb publication page



Dataset of GWAS-identified variants underlying venous thromboembolism susceptibility and linkage to cancer aggressiveness.

Data In Brief
Tavares, Valéria V; Pinto, Ricardo R; Assis, Joana J; Pereira, Deolinda D; Medeiros, Rui R
Publication Date: 2020-06

Variant appearance in text: rs687621
PubMed Link: 32258274
Variant Present in the following documents:
  • Main text
View BVdb publication page



The cartilage matrisome in adolescent idiopathic scoliosis.

Bone Research
Wise, Carol A CA; Sepich, Diane D; Ushiki, Aki A; Khanshour, Anas M AM; Kidane, Yared H YH; Makki, Nadja N; Gurnett, Christina A CA; Gray, Ryan S RS; Rios, Jonathan J JJ; Ahituv, Nadav N; Solnica-Krezel, Lila L
Publication Date: 2020

Variant appearance in text: rs687621
PubMed Link: 32195011
Variant Present in the following documents:
  • Main text
View BVdb publication page



Dysregulated Antibody, Natural Killer Cell and Immune Mediator Profiles in Autoimmune Thyroid Diseases.

Cells
Martin, Tiphaine C TC; Ilieva, Kristina M KM; Visconti, Alessia A; Beaumont, Michelle M; Kiddle, Steven J SJ; Dobson, Richard J B RJB; Mangino, Massimo M; Lim, Ee Mun EM; Pezer, Marija M; Steves, Claire J CJ; Bell, Jordana T JT; Wilson, Scott G SG; Lauc, Gordan G; Roederer, Mario M; Walsh, John P JP; Spector, Tim D TD; Karagiannis, Sophia N SN
Publication Date: 2020-03-09

Variant appearance in text: rs687621
PubMed Link: 32182948
Variant Present in the following documents:
  • Main text
  • cells-09-00665.pdf
View BVdb publication page



A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness.

Human Genetics
Nudel, Ron R; Appadurai, Vivek V; Schork, Andrew J AJ; Buil, Alfonso A; Bybjerg-Grauholm, Jonas J; Børglum, Anders D AD; Daly, Mark J MJ; Mors, Ole O; Hougaard, David M DM; Mortensen, Preben Bo PB; Werge, Thomas T; Nordentoft, Merete M; Thompson, Wesley K WK; Benros, Michael E ME
Publication Date: 2020-05

Variant appearance in text: rs687621
PubMed Link: 32152699
Variant Present in the following documents:
  • Main text
View BVdb publication page



A Transcriptome-Wide Association Study Identifies Novel Candidate Susceptibility Genes for Pancreatic Cancer.

Journal Of The National Cancer Institute
Zhong, Jun J; Jermusyk, Ashley A; Wu, Lang L; Hoskins, Jason W JW; Collins, Irene I; Mocci, Evelina E; Zhang, Mingfeng M; Song, Lei L; Chung, Charles C CC; Zhang, Tongwu T; Xiao, Wenming W; Albanes, Demetrius D; Andreotti, Gabriella G; Arslan, Alan A AA; Babic, Ana A; Bamlet, William R WR; Beane-Freeman, Laura L; Berndt, Sonja S; Borgida, Ayelet A; Bracci, Paige M PM; Brais, Lauren L; Brennan, Paul P; Bueno-de-Mesquita, Bas B; Buring, Julie J; Canzian, Federico F; Childs, Erica J EJ; Cotterchio, Michelle M; Du, Mengmeng M; Duell, Eric J EJ; Fuchs, Charles C; Gallinger, Steven S; Gaziano, J Michael JM; Giles, Graham G GG; Giovannucci, Edward E; Goggins, Michael M; Goodman, Gary E GE; Goodman, Phyllis J PJ; Haiman, Christopher C; Hartge, Patricia P; Hasan, Manal M; Helzlsouer, Kathy J KJ; Holly, Elizabeth A EA; Klein, Eric A EA; Kogevinas, Manolis M; Kurtz, Robert J RJ; LeMarchand, Loic L; Malats, Núria N; Männistö, Satu S; Milne, Roger R; Neale, Rachel E RE; Ng, Kimmie K; Obazee, Ofure O; Oberg, Ann L AL; Orlow, Irene I; Patel, Alpa V AV; Peters, Ulrike U; Porta, Miquel M; Rothman, Nathaniel N; Scelo, Ghislaine G; Sesso, Howard D HD; Severi, Gianluca G; Sieri, Sabina S; Silverman, Debra D; Sund, Malin M; Tjønneland, Anne A; Thornquist, Mark D MD; Tobias, Geoffrey S GS; Trichopoulou, Antonia A; Van Den Eeden, Stephen K SK; Visvanathan, Kala K; Wactawski-Wende, Jean J; Wentzensen, Nicolas N; White, Emily E; Yu, Herbert H; Yuan, Chen C; Zeleniuch-Jacquotte, Anne A; Hoover, Robert R; Brown, Kevin K; Kooperberg, Charles C; Risch, Harvey A HA; Jacobs, Eric J EJ; Li, Donghui D; Yu, Kai K; Shu, Xiao-Ou XO; Chanock, Stephen J SJ; Wolpin, Brian M BM; Stolzenberg-Solomon, Rachael Z RZ; Chatterjee, Nilanjan N; Klein, Alison P AP; Smith, Jill P JP; Kraft, Peter P; Shi, Jianxin J; Petersen, Gloria M GM; Zheng, Wei W; Amundadottir, Laufey T LT
Publication Date: 2020-10-01

Variant appearance in text: rs687621
PubMed Link: 31917448
Variant Present in the following documents:
  • Main text
View BVdb publication page



The transferability of lipid loci across African, Asian and European cohorts.

Nature Communications
Kuchenbaecker, Karoline K; Telkar, Nikita N; Reiker, Theresa T; Walters, Robin G RG; Lin, Kuang K; Eriksson, Anders A; Gurdasani, Deepti D; Gilly, Arthur A; Southam, Lorraine L; Tsafantakis, Emmanouil E; Karaleftheri, Maria M; Seeley, Janet J; Kamali, Anatoli A; Asiki, Gershim G; Millwood, Iona Y IY; Holmes, Michael M; Du, Huaidong H; Guo, Yu Y; Kumari, Meena M; Dedoussis, George G; Li, Liming L; Chen, Zhengming Z; Sandhu, Manjinder S MS; Zeggini, Eleftheria E; ,
Publication Date: 2019-09-24

Variant appearance in text: rs687621
PubMed Link: 31551420
Variant Present in the following documents:
  • 41467_2019_12026_MOESM1_ESM.pdf
View BVdb publication page



Influence of ABO Locus on PFA-100 Collagen-ADP Closure Time Is Not Totally Dependent on the Von Willebrand Factor. Results of a GWAS on GAIT-2 Project Phenotypes.

International Journal Of Molecular Sciences
Pujol-Moix, Núria N; Martinez-Perez, Angel A; Sabater-Lleal, Maria M; Llobet, Dolors D; Vilalta, Noèlia N; Hamsten, Anders A; Souto, Joan Carles JC; Soria, José Manuel JM
Publication Date: 2019-06-30

Variant appearance in text: rs687621
PubMed Link: 31262040
Variant Present in the following documents:
  • Main text
  • ijms-20-03221.pdf
View BVdb publication page



A multimodal approach to cardiovascular risk stratification in patients with type 2 diabetes incorporating retinal, genomic and clinical features.

Scientific Reports
Fetit, Ahmed E AE; Doney, Alexander S AS; Hogg, Stephen S; Wang, Ruixuan R; MacGillivray, Tom T; Wardlaw, Joanna M JM; Doubal, Fergus N FN; McKay, Gareth J GJ; McKenna, Stephen S; Trucco, Emanuele E
Publication Date: 2019-03-05

Variant appearance in text: rs687621
PubMed Link: 30837638
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_40403.pdf
View BVdb publication page



Genome-Wide Association Transethnic Meta-Analyses Identifies Novel Associations Regulating Coagulation Factor VIII and von Willebrand Factor Plasma Levels.

Circulation
Sabater-Lleal, Maria M; Huffman, Jennifer E JE; de Vries, Paul S PS; Marten, Jonathan J; Mastrangelo, Michael A MA; Song, Ci C; Pankratz, Nathan N; Ward-Caviness, Cavin K CK; Yanek, Lisa R LR; Trompet, Stella S; Delgado, Graciela E GE; Guo, Xiuqing X; Bartz, Traci M TM; Martinez-Perez, Angel A; Germain, Marine M; de Haan, Hugoline G HG; Ozel, Ayse B AB; Polasek, Ozren O; Smith, Albert V AV; Eicher, John D JD; Reiner, Alex P AP; Tang, Weihong W; Davies, Neil M NM; Stott, David J DJ; Rotter, Jerome I JI; Tofler, Geoffrey H GH; Boerwinkle, Eric E; de Maat, Moniek P M MPM; Kleber, Marcus E ME; Welsh, Paul P; Brody, Jennifer A JA; Chen, Ming-Huei MH; Vaidya, Dhananjay D; Soria, José Manuel JM; Suchon, Pierre P; van Hylckama Vlieg, Astrid A; Desch, Karl C KC; Kolcic, Ivana I; Joshi, Peter K PK; Launer, Lenore J LJ; Harris, Tamara B TB; Campbell, Harry H; Rudan, Igor I; Becker, Diane M DM; Li, Jun Z JZ; Rivadeneira, Fernando F; Uitterlinden, André G AG; Hofman, Albert A; Franco, Oscar H OH; Cushman, Mary M; Psaty, Bruce M BM; Morange, Pierre-Emmanuel PE; McKnight, Barbara B; Chong, Michael R MR; Fernandez-Cadenas, Israel I; Rosand, Jonathan J; Lindgren, Arne A; , ; Gudnason, Vilmundur V; Wilson, James F JF; Hayward, Caroline C; Ginsburg, David D; Fornage, Myriam M; Rosendaal, Frits R FR; Souto, Juan Carlos JC; Becker, Lewis C LC; Jenny, Nancy S NS; März, Winfried W; Jukema, J Wouter JW; Dehghan, Abbas A; Trégouët, David-Alexandre DA; Morrison, Alanna C AC; Johnson, Andrew D AD; O'Donnell, Christopher J CJ; Strachan, David P DP; Lowenstein, Charles J CJ; Smith, Nicholas L NL
Publication Date: 2019-01-29

Variant appearance in text: rs687621
PubMed Link: 30586737
Variant Present in the following documents:
  • Main text
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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: ABO: 99-288T>C; rs687621
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_5.xlsx, sheet 1
  • Table_6.xlsx, sheet 1
View BVdb publication page



Interaction of a genetic risk score with physical activity, physical inactivity, and body mass index in relation to venous thromboembolism risk.

Genetic Epidemiology
Kim, Jihye J; Kraft, Peter P; Hagan, Kaitlin A KA; Harrington, Laura B LB; Lindstroem, Sara S; Kabrhel, Christopher C
Publication Date: 2018-06

Variant appearance in text: rs687621
PubMed Link: 29520861
Variant Present in the following documents:
  • Main text
View BVdb publication page



Mendelian Randomization Analysis Identifies CpG Sites as Putative Mediators for Genetic Influences on Cardiovascular Disease Risk.

American Journal Of Human Genetics
Richardson, Tom G TG; Zheng, Jie J; Davey Smith, George G; Timpson, Nicholas J NJ; Gaunt, Tom R TR; Relton, Caroline L CL; Hemani, Gibran G
Publication Date: 2017-10-05

Variant appearance in text: rs687621
PubMed Link: 28985495
Variant Present in the following documents:
  • Main text
  • main.pdf
  • mmc3.pdf
View BVdb publication page



Risk prediction of developing venous thrombosis in combined oral contraceptive users.

Plos One
McDaid, Aaron A; Logette, Emmanuelle E; Buchillier, Valérie V; Muriset, Maude M; Suchon, Pierre P; Pache, Thierry Daniel TD; Tanackovic, Goranka G; Kutalik, Zoltán Z; Michaud, Joëlle J
Publication Date: 2017

Variant appearance in text: rs687621
PubMed Link: 28750087
Variant Present in the following documents:
  • Main text
  • pone.0182041.pdf
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Genetic Drivers of von Willebrand Factor Levels in an Ischemic Stroke Population and Association With Risk for Recurrent Stroke.

Stroke
Williams, Stephen R SR; Hsu, Fang-Chi FC; Keene, Keith L KL; Chen, Wei-Min WM; Dzhivhuho, Godfrey G; Rowles, Joe L JL; Southerland, Andrew M AM; Furie, Karen L KL; Rich, Stephen S SS; Worrall, Bradford B BB; Sale, Michèle M MM; ,
Publication Date: 2017-06

Variant appearance in text: rs687621
PubMed Link: 28495826
Variant Present in the following documents:
  • Main text
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Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.

Nature Genetics
Surendran, Praveen P; Drenos, Fotios F; Young, Robin R; Warren, Helen H; Cook, James P JP; Manning, Alisa K AK; Grarup, Niels N; Sim, Xueling X; Barnes, Daniel R DR; Witkowska, Kate K; Staley, James R JR; Tragante, Vinicius V; Tukiainen, Taru T; Yaghootkar, Hanieh H; Masca, Nicholas N; Freitag, Daniel F DF; Ferreira, Teresa T; Giannakopoulou, Olga O; Tinker, Andrew A; Harakalova, Magdalena M; Mihailov, Evelin E; Liu, Chunyu C; Kraja, Aldi T AT; Fallgaard Nielsen, Sune S; Rasheed, Asif A; Samuel, Maria M; Zhao, Wei W; Bonnycastle, Lori L LL; Jackson, Anne U AU; Narisu, Narisu N; Swift, Amy J AJ; Southam, Lorraine L; Marten, Jonathan J; Huyghe, Jeroen R JR; Stančáková, Alena A; Fava, Cristiano C; Ohlsson, Therese T; Matchan, Angela A; Stirrups, Kathleen E KE; Bork-Jensen, Jette J; Gjesing, Anette P AP; Kontto, Jukka J; Perola, Markus M; Shaw-Hawkins, Susan S; Havulinna, Aki S AS; Zhang, He H; Donnelly, Louise A LA; Groves, Christopher J CJ; Rayner, N William NW; Neville, Matt J MJ; Robertson, Neil R NR; Yiorkas, Andrianos M AM; Herzig, Karl-Heinz KH; Kajantie, Eero E; Zhang, Weihua W; Willems, Sara M SM; Lannfelt, Lars L; Malerba, Giovanni G; Soranzo, Nicole N; Trabetti, Elisabetta E; Verweij, Niek N; Evangelou, Evangelos E; Moayyeri, Alireza A; Vergnaud, Anne-Claire AC; Nelson, Christopher P CP; Poveda, Alaitz A; Varga, Tibor V TV; Caslake, Muriel M; de Craen, Anton Jm AJ; Trompet, Stella S; Luan, Jian'an J; Scott, Robert A RA; Harris, Sarah E SE; Liewald, David Cm DC; Marioni, Riccardo R; Menni, Cristina C; Farmaki, Aliki-Eleni AE; Hallmans, Göran G; Renström, Frida F; Huffman, Jennifer E JE; Hassinen, Maija M; Burgess, Stephen S; Vasan, Ramachandran S RS; Felix, Janine F JF; , ; Uria-Nickelsen, Maria M; Malarstig, Anders A; Reily, Dermot F DF; Hoek, Maarten M; Vogt, Thomas T; Lin, Honghuang H; Lieb, Wolfgang W; , ; Traylor, Matthew M; Markus, Hugh F HF; , ; Highland, Heather M HM; Justice, Anne E AE; Marouli, Eirini E; , ; Lindström, Jaana J; Uusitupa, Matti M; Komulainen, Pirjo P; Lakka, Timo A TA; Rauramaa, Rainer R; Polasek, Ozren O; Rudan, Igor I; Rolandsson, Olov O; Franks, Paul W PW; Dedoussis, George G; Spector, Timothy D TD; , ; Jousilahti, Pekka P; Männistö, Satu S; Deary, Ian J IJ; Starr, John M JM; Langenberg, Claudia C; Wareham, Nick J NJ; Brown, Morris J MJ; Dominiczak, Anna F AF; Connell, John M JM; Jukema, J Wouter JW; Sattar, Naveed N; Ford, Ian I; Packard, Chris J CJ; Esko, Tõnu T; Mägi, Reedik R; Metspalu, Andres A; de Boer, Rudolf A RA; van der Meer, Peter P; van der Harst, Pim P; , ; Gambaro, Giovanni G; Ingelsson, Erik E; Lind, Lars L; de Bakker, Paul Iw PI; Numans, Mattijs E ME; Brandslund, Ivan I; Christensen, Cramer C; Petersen, Eva Rb ER; Korpi-Hyövälti, Eeva E; Oksa, Heikki H; Chambers, John C JC; Kooner, Jaspal S JS; Blakemore, Alexandra If AI; Franks, Steve S; Jarvelin, Marjo-Riitta MR; Husemoen, Lise L LL; Linneberg, Allan A; Skaaby, Tea T; Thuesen, Betina B; Karpe, Fredrik F; Tuomilehto, Jaakko J; Doney, Alex Sf AS; Morris, Andrew D AD; Palmer, Colin Na CN; Holmen, Oddgeir Lingaas OL; Hveem, Kristian K; Willer, Cristen J CJ; Tuomi, Tiinamaija T; Groop, Leif L; Käräjämäki, AnneMari A; Palotie, Aarno A; Ripatti, Samuli S; Salomaa, Veikko V; Alam, Dewan S DS; Shafi Majumder, Abdulla Al AA; Di Angelantonio, Emanuele E; Chowdhury, Rajiv R; McCarthy, Mark I MI; Poulter, Neil N; Stanton, Alice V AV; Sever, Peter P; Amouyel, Philippe P; Arveiler, Dominique D; Blankenberg, Stefan S; Ferrières, Jean J; Kee, Frank F; Kuulasmaa, Kari K; Müller-Nurasyid, Martina M; Veronesi, Giovanni G; Virtamo, Jarmo J; Deloukas, Panos P; , ; Elliott, Paul P; , ; Zeggini, Eleftheria E; Kathiresan, Sekar S; Melander, Olle O; Kuusisto, Johanna J; Laakso, Markku M; Padmanabhan, Sandosh S; Porteous, David D; Hayward, Caroline C; Scotland, Generation G; Collins, Francis S FS; Mohlke, Karen L KL; Hansen, Torben T; Pedersen, Oluf O; Boehnke, Michael M; Stringham, Heather M HM; , ; Frossard, Philippe P; Newton-Cheh, Christopher C; , ; Tobin, Martin D MD; Nordestgaard, Børge Grønne BG; , ; , ; , ; , ; Caulfield, Mark J MJ; Mahajan, Anubha A; Morris, Andrew P AP; Tomaszewski, Maciej M; Samani, Nilesh J NJ; Saleheen, Danish D; Asselbergs, Folkert W FW; Lindgren, Cecilia M CM; Danesh, John J; Wain, Louise V LV; Butterworth, Adam S AS; Howson, Joanna Mm JM; Munroe, Patricia B PB
Publication Date: 2016-10

Variant appearance in text: rs687621
PubMed Link: 27618447
Variant Present in the following documents:
  • Main text
  • NIHMS69533-supplement-Supplementary_Tables.xlsx, sheet 16
  • NIHMS69533-supplement-Supplementary_Tables.xlsx, sheet 5
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Interactions of established risk factors and a GWAS-based genetic risk score on the risk of venous thromboembolism.

Thrombosis And Haemostasis
Crous-Bou, Marta M; De Vivo, Immaculata I; Camargo, Carlos A CA; Varraso, Raphaëlle R; Grodstein, Francine F; Jensen, Majken K MK; Kraft, Peter P; Goldhaber, Samuel Z SZ; Lindström, Sara S; Kabrhel, Christopher C
Publication Date: 2016-09-27

Variant appearance in text: rs687621
PubMed Link: 27305932
Variant Present in the following documents:
  • Main text
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Novel genetic predictors of venous thromboembolism risk in African Americans.

Blood
Hernandez, Wenndy W; Gamazon, Eric R ER; Smithberger, Erin E; O'Brien, Travis J TJ; Harralson, Arthur F AF; Tuck, Matthew M; Barbour, April A; Kittles, Rick A RA; Cavallari, Larisa H LH; Perera, Minoli A MA
Publication Date: 2016-04-14

Variant appearance in text: rs687621
PubMed Link: 26888256
Variant Present in the following documents:
  • Main text
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Genome-Wide Association Study Identifies That the ABO Blood Group System Influences Interleukin-10 Levels and the Risk of Clinical Events in Patients with Acute Coronary Syndrome.

Plos One
Johansson, Åsa Å; Alfredsson, Jenny J; Eriksson, Niclas N; Wallentin, Lars L; Siegbahn, Agneta A
Publication Date: 2015

Variant appearance in text: rs687621
PubMed Link: 26600159
Variant Present in the following documents:
  • Main text
  • pone.0142518.pdf
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Dissecting the genetic determinants of hemostasis and thrombosis.

Current Opinion In Hematology
Desch, Karl C KC
Publication Date: 2015-09

Variant appearance in text: rs687621
PubMed Link: 26248003
Variant Present in the following documents:
  • Main text
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Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility.

Nature Communications
Wessel, Jennifer J; Chu, Audrey Y AY; Willems, Sara M SM; Wang, Shuai S; Yaghootkar, Hanieh H; Brody, Jennifer A JA; Dauriz, Marco M; Hivert, Marie-France MF; Raghavan, Sridharan S; Lipovich, Leonard L; Hidalgo, Bertha B; Fox, Keolu K; Huffman, Jennifer E JE; An, Ping P; Lu, Yingchang Y; Rasmussen-Torvik, Laura J LJ; Grarup, Niels N; Ehm, Margaret G MG; Li, Li L; Baldridge, Abigail S AS; Stančáková, Alena A; Abrol, Ravinder R; Besse, Céline C; Boland, Anne A; Bork-Jensen, Jette J; Fornage, Myriam M; Freitag, Daniel F DF; Garcia, Melissa E ME; Guo, Xiuqing X; Hara, Kazuo K; Isaacs, Aaron A; Jakobsdottir, Johanna J; Lange, Leslie A LA; Layton, Jill C JC; Li, Man M; Hua Zhao, Jing J; Meidtner, Karina K; Morrison, Alanna C AC; Nalls, Mike A MA; Peters, Marjolein J MJ; Sabater-Lleal, Maria M; Schurmann, Claudia C; Silveira, Angela A; Smith, Albert V AV; Southam, Lorraine L; Stoiber, Marcus H MH; Strawbridge, Rona J RJ; Taylor, Kent D KD; Varga, Tibor V TV; Allin, Kristine H KH; Amin, Najaf N; Aponte, Jennifer L JL; Aung, Tin T; Barbieri, Caterina C; Bihlmeyer, Nathan A NA; Boehnke, Michael M; Bombieri, Cristina C; Bowden, Donald W DW; Burns, Sean M SM; Chen, Yuning Y; Chen, Yii-DerI YD; Cheng, Ching-Yu CY; Correa, Adolfo A; Czajkowski, Jacek J; Dehghan, Abbas A; Ehret, Georg B GB; Eiriksdottir, Gudny G; Escher, Stefan A SA; Farmaki, Aliki-Eleni AE; Frånberg, Mattias M; Gambaro, Giovanni G; Giulianini, Franco F; Goddard, William A WA; Goel, Anuj A; Gottesman, Omri O; Grove, Megan L ML; Gustafsson, Stefan S; Hai, Yang Y; Hallmans, Göran G; Heo, Jiyoung J; Hoffmann, Per P; Ikram, Mohammad K MK; Jensen, Richard A RA; Jørgensen, Marit E ME; Jørgensen, Torben T; Karaleftheri, Maria M; Khor, Chiea C CC; Kirkpatrick, Andrea A; Kraja, Aldi T AT; Kuusisto, Johanna J; Lange, Ethan M EM; Lee, I T IT; Lee, Wen-Jane WJ; Leong, Aaron A; Liao, Jiemin J; Liu, Chunyu C; Liu, Yongmei Y; Lindgren, Cecilia M CM; Linneberg, Allan A; Malerba, Giovanni G; Mamakou, Vasiliki V; Marouli, Eirini E; Maruthur, Nisa M NM; Matchan, Angela A; McKean-Cowdin, Roberta R; McLeod, Olga O; Metcalf, Ginger A GA; Mohlke, Karen L KL; Muzny, Donna M DM; Ntalla, Ioanna I; Palmer, Nicholette D ND; Pasko, Dorota D; Peter, Andreas A; Rayner, Nigel W NW; Renström, Frida F; Rice, Ken K; Sala, Cinzia F CF; Sennblad, Bengt B; Serafetinidis, Ioannis I; Smith, Jennifer A JA; Soranzo, Nicole N; Speliotes, Elizabeth K EK; Stahl, Eli A EA; Stirrups, Kathleen K; Tentolouris, Nikos N; Thanopoulou, Anastasia A; Torres, Mina M; Traglia, Michela M; Tsafantakis, Emmanouil E; Javad, Sundas S; Yanek, Lisa R LR; Zengini, Eleni E; Becker, Diane M DM; Bis, Joshua C JC; Brown, James B JB; Cupples, L Adrienne LA; Hansen, Torben T; Ingelsson, Erik E; Karter, Andrew J AJ; Lorenzo, Carlos C; Mathias, Rasika A RA; Norris, Jill M JM; Peloso, Gina M GM; Sheu, Wayne H-H WH; Toniolo, Daniela D; Vaidya, Dhananjay D; Varma, Rohit R; Wagenknecht, Lynne E LE; Boeing, Heiner H; Bottinger, Erwin P EP; Dedoussis, George G; Deloukas, Panos P; Ferrannini, Ele E; Franco, Oscar H OH; Franks, Paul W PW; Gibbs, Richard A RA; Gudnason, Vilmundur V; Hamsten, Anders A; Harris, Tamara B TB; Hattersley, Andrew T AT; Hayward, Caroline C; Hofman, Albert A; Jansson, Jan-Håkan JH; Langenberg, Claudia C; Launer, Lenore J LJ; Levy, Daniel D; Oostra, Ben A BA; O'Donnell, Christopher J CJ; O'Rahilly, Stephen S; Padmanabhan, Sandosh S; Pankow, James S JS; Polasek, Ozren O; Province, Michael A MA; Rich, Stephen S SS; Ridker, Paul M PM; Rudan, Igor I; Schulze, Matthias B MB; Smith, Blair H BH; Uitterlinden, André G AG; Walker, Mark M; Watkins, Hugh H; Wong, Tien Y TY; Zeggini, Eleftheria E; , ; Laakso, Markku M; Borecki, Ingrid B IB; Chasman, Daniel I DI; Pedersen, Oluf O; Psaty, Bruce M BM; Tai, E Shyong ES; van Duijn, Cornelia M CM; Wareham, Nicholas J NJ; Waterworth, Dawn M DM; Boerwinkle, Eric E; Kao, W H Linda WH; Florez, Jose C JC; Loos, Ruth J F RJ; Wilson, James G JG; Frayling, Timothy M TM; Siscovick, David S DS; Dupuis, Josée J; Rotter, Jerome I JI; Meigs, James B JB; Scott, Robert A RA; Goodarzi, Mark O MO
Publication Date: 2015-01-29

Variant appearance in text: rs687621
PubMed Link: 25631608
Variant Present in the following documents:
  • ncomms6897-s1.pdf
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A genetic association study of activated partial thromboplastin time in European Americans and African Americans: the ARIC Study.

Human Molecular Genetics
Weng, Lu-Chen LC; Cushman, Mary M; Pankow, James S JS; Basu, Saonli S; Boerwinkle, Eric E; Folsom, Aaron R AR; Tang, Weihong W
Publication Date: 2015-04-15

Variant appearance in text: rs687621
PubMed Link: 25552651
Variant Present in the following documents:
  • Main text
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Single nucleotide polymorphisms with cis-regulatory effects on long non-coding transcripts in human primary monocytes.

Plos One
Almlöf, Jonas Carlsson JC; Lundmark, Per P; Lundmark, Anders A; Ge, Bing B; Pastinen, Tomi T; , ; Goodall, Alison H AH; Cambien, François F; Deloukas, Panos P; Ouwehand, Willem H WH; Syvänen, Ann-Christine AC
Publication Date: 2014

Variant appearance in text: rs687621
PubMed Link: 25025429
Variant Present in the following documents:
  • Main text
  • pone.0102612.pdf
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Genetic associations with expression for genes implicated in GWAS studies for atherosclerotic cardiovascular disease and blood phenotypes.

Human Molecular Genetics
Zhang, Xiaoling X; Johnson, Andrew D AD; Hendricks, Audrey E AE; Hwang, Shih-Jen SJ; Tanriverdi, Kahraman K; Ganesh, Santhi K SK; Smith, Nicholas L NL; Peyser, Patricia A PA; Freedman, Jane E JE; O'Donnell, Christopher J CJ
Publication Date: 2014-02-01

Variant appearance in text: rs687621
PubMed Link: 24057673
Variant Present in the following documents:
  • Main text
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A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.

Genetic Epidemiology
Tang, Weihong W; Teichert, Martina M; Chasman, Daniel I DI; Heit, John A JA; Morange, Pierre-Emmanuel PE; Li, Guo G; Pankratz, Nathan N; Leebeek, Frank W FW; Paré, Guillaume G; de Andrade, Mariza M; Tzourio, Christophe C; Psaty, Bruce M BM; Basu, Saonli S; Ruiter, Rikje R; Rose, Lynda L; Armasu, Sebastian M SM; Lumley, Thomas T; Heckbert, Susan R SR; Uitterlinden, André G AG; Lathrop, Mark M; Rice, Kenneth M KM; Cushman, Mary M; Hofman, Albert A; Lambert, Jean-Charles JC; Glazer, Nicole L NL; Pankow, James S JS; Witteman, Jacqueline C JC; Amouyel, Philippe P; Bis, Joshua C JC; Bovill, Edwin G EG; Kong, Xiaoxiao X; Tracy, Russell P RP; Boerwinkle, Eric E; Rotter, Jerome I JI; Trégouët, David-Alexandre DA; Loth, Daan W DW; Stricker, Bruno H Ch BHC; Ridker, Paul M PM; Folsom, Aaron R AR; Smith, Nicholas L NL
Publication Date: 2013-07

Variant appearance in text: rs687621
PubMed Link: 23650146
Variant Present in the following documents:
  • Main text
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ABO Blood Groups and Cardiovascular Diseases.

International Journal Of Vascular Medicine
Zhang, Hanrui H; Mooney, Ciarán J CJ; Reilly, Muredach P MP
Publication Date: 2012

Variant appearance in text: rs687621
PubMed Link: 23133757
Variant Present in the following documents:
  • Main text
  • IJVM2012-641917.pdf
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Prioritizing genetic variants for causality on the basis of preferential linkage disequilibrium.

American Journal Of Human Genetics
Zhu, Qianqian Q; Ge, Dongliang D; Heinzen, Erin L EL; Dickson, Samuel P SP; Urban, Thomas J TJ; Zhu, Mingfu M; Maia, Jessica M JM; He, Min M; Zhao, Qian Q; Shianna, Kevin V KV; Goldstein, David B DB
Publication Date: 2012-09-07

Variant appearance in text: rs687621
PubMed Link: 22939045
Variant Present in the following documents:
  • Main text
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Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.

American Journal Of Human Genetics
Tang, Weihong W; Schwienbacher, Christine C; Lopez, Lorna M LM; Ben-Shlomo, Yoav Y; Oudot-Mellakh, Tiphaine T; Johnson, Andrew D AD; Samani, Nilesh J NJ; Basu, Saonli S; Gögele, Martin M; Davies, Gail G; Lowe, Gordon D O GD; Tregouet, David-Alexandre DA; Tan, Adrian A; Pankow, James S JS; Tenesa, Albert A; Levy, Daniel D; Volpato, Claudia B CB; Rumley, Ann A; Gow, Alan J AJ; Minelli, Cosetta C; Yarnell, John W G JW; Porteous, David J DJ; Starr, John M JM; Gallacher, John J; Boerwinkle, Eric E; Visscher, Peter M PM; Pramstaller, Peter P PP; Cushman, Mary M; Emilsson, Valur V; Plump, Andrew S AS; Matijevic, Nena N; Morange, Pierre-Emmanuel PE; Deary, Ian J IJ; Hicks, Andrew A AA; Folsom, Aaron R AR
Publication Date: 2012-07-13

Variant appearance in text: rs687621
PubMed Link: 22703881
Variant Present in the following documents:
  • Main text
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A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains.

Plos Genetics
Avery, Christy L CL; He, Qianchuan Q; North, Kari E KE; Ambite, Jose L JL; Boerwinkle, Eric E; Fornage, Myriam M; Hindorff, Lucia A LA; Kooperberg, Charles C; Meigs, James B JB; Pankow, James S JS; Pendergrass, Sarah A SA; Psaty, Bruce M BM; Ritchie, Marylyn D MD; Rotter, Jerome I JI; Taylor, Kent D KD; Wilkens, Lynne R LR; Heiss, Gerardo G; Lin, Dan Yu DY
Publication Date: 2011-10

Variant appearance in text: rs687621
PubMed Link: 22022282
Variant Present in the following documents:
  • Main text
  • pgen.1002322.pdf
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Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies.

Lancet (London, England)
Reilly, Muredach P MP; Li, Mingyao M; He, Jing J; Ferguson, Jane F JF; Stylianou, Ioannis M IM; Mehta, Nehal N NN; Burnett, Mary Susan MS; Devaney, Joseph M JM; Knouff, Christopher W CW; Thompson, John R JR; Horne, Benjamin D BD; Stewart, Alexandre F R AF; Assimes, Themistocles L TL; Wild, Philipp S PS; Allayee, Hooman H; Nitschke, Patrick Linsel PL; Patel, Riyaz S RS; , ; , ; Martinelli, Nicola N; Girelli, Domenico D; Quyyumi, Arshed A AA; Anderson, Jeffrey L JL; Erdmann, Jeanette J; Hall, Alistair S AS; Schunkert, Heribert H; Quertermous, Thomas T; Blankenberg, Stefan S; Hazen, Stanley L SL; Roberts, Robert R; Kathiresan, Sekar S; Samani, Nilesh J NJ; Epstein, Stephen E SE; Rader, Daniel J DJ
Publication Date: 2011-01-29

Variant appearance in text: rs687621
PubMed Link: 21239051
Variant Present in the following documents:
  • Main text
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Genetic variation associated with plasma von Willebrand factor levels and the risk of incident venous thrombosis.

Blood
Smith, Nicholas L NL; Rice, Kenneth M KM; Bovill, Edwin G EG; Cushman, Mary M; Bis, Joshua C JC; McKnight, Barbara B; Lumley, Thomas T; Glazer, Nicole L NL; van Hylckama Vlieg, Astrid A; Tang, Weihong W; Dehghan, Abbas A; Strachan, David P DP; O'Donnell, Christopher J CJ; Rotter, Jerome I JI; Heckbert, Susan R SR; Psaty, Bruce M BM; Rosendaal, Frits R FR
Publication Date: 2011-06-02

Variant appearance in text: rs687621
PubMed Link: 21163921
Variant Present in the following documents:
  • Main text
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Genome-wide association study identifies variants in the ABO locus associated with susceptibility to pancreatic cancer.

Nature Genetics
Amundadottir, Laufey L; Kraft, Peter P; Stolzenberg-Solomon, Rachael Z RZ; Fuchs, Charles S CS; Petersen, Gloria M GM; Arslan, Alan A AA; Bueno-de-Mesquita, H Bas HB; Gross, Myron M; Helzlsouer, Kathy K; Jacobs, Eric J EJ; LaCroix, Andrea A; Zheng, Wei W; Albanes, Demetrius D; Bamlet, William W; Berg, Christine D CD; Berrino, Franco F; Bingham, Sheila S; Buring, Julie E JE; Bracci, Paige M PM; Canzian, Federico F; Clavel-Chapelon, Françoise F; Clipp, Sandra S; Cotterchio, Michelle M; de Andrade, Mariza M; Duell, Eric J EJ; Fox, John W JW; Gallinger, Steven S; Gaziano, J Michael JM; Giovannucci, Edward L EL; Goggins, Michael M; González, Carlos A CA; Hallmans, Göran G; Hankinson, Susan E SE; Hassan, Manal M; Holly, Elizabeth A EA; Hunter, David J DJ; Hutchinson, Amy A; Jackson, Rebecca R; Jacobs, Kevin B KB; Jenab, Mazda M; Kaaks, Rudolf R; Klein, Alison P AP; Kooperberg, Charles C; Kurtz, Robert C RC; Li, Donghui D; Lynch, Shannon M SM; Mandelson, Margaret M; McWilliams, Robert R RR; Mendelsohn, Julie B JB; Michaud, Dominique S DS; Olson, Sara H SH; Overvad, Kim K; Patel, Alpa V AV; Peeters, Petra H M PH; Rajkovic, Aleksandar A; Riboli, Elio E; Risch, Harvey A HA; Shu, Xiao-Ou XO; Thomas, Gilles G; Tobias, Geoffrey S GS; Trichopoulos, Dimitrios D; Van Den Eeden, Stephen K SK; Virtamo, Jarmo J; Wactawski-Wende, Jean J; Wolpin, Brian M BM; Yu, Herbert H; Yu, Kai K; Zeleniuch-Jacquotte, Anne A; Chanock, Stephen J SJ; Hartge, Patricia P; Hoover, Robert N RN
Publication Date: 2009-09

Variant appearance in text: rs687621
PubMed Link: 19648918
Variant Present in the following documents:
  • Main text
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Novel association of ABO histo-blood group antigen with soluble ICAM-1: results of a genome-wide association study of 6,578 women.

Plos Genetics
Paré, Guillaume G; Chasman, Daniel I DI; Kellogg, Mark M; Zee, Robert Y L RY; Rifai, Nader N; Badola, Sunita S; Miletich, Joseph P JP; Ridker, Paul M PM
Publication Date: 2008-07-04

Variant appearance in text: rs687621
PubMed Link: 18604267
Variant Present in the following documents:
  • Main text
  • pgen.1000118.pdf
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