POLR1D c.*49C>T

Variant ID: 13-28197436-C-T

NM_015972.3(POLR1D):c.*49C>T

This variant was identified in 30 publications

View GRCh38 version.




Publications:


Integrative proteomic characterization of adenocarcinoma of esophagogastric junction.

Nature Communications
Li, Shengli S; Yuan, Li L; Xu, Zhi-Yuan ZY; Xu, Jing-Li JL; Chen, Gui-Ping GP; Guan, Xiaoqing X; Pan, Guang-Zhao GZ; Hu, Can C; Dong, Jinyun J; Du, Yi-An YA; Yang, Li-Tao LT; Ni, Mao-Wei MW; Jiang, Rui-Bin RB; Zhu, Xiu X; Lv, Hang H; Xu, Han-Dong HD; Zhang, Sheng-Jie SJ; Qin, Jiang-Jiang JJ; Cheng, Xiang-Dong XD
Publication Date: 2023-02-11

Variant appearance in text: rs7097
PubMed Link: 36774361
Variant Present in the following documents:
  • 41467_2023_36462_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Mutation analysis of the WFS1 gene in a Chinese family with autosomal-dominant non-syndrome deafness.

Scientific Reports
Zhao, Jing J; Zhang, Siqi S; Jiang, Yuan Y; Liu, Yan Y; Wang, Jiantao J; Zhu, QingWen Q
Publication Date: 2022-12-23

Variant appearance in text: rs7097
PubMed Link: 36564540
Variant Present in the following documents:
  • 41598_2022_26850_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: rs7097
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Mutation analysis of the GSDME gene in a Chinese family with non-syndromic hearing loss.

Plos One
Lei, Peiliang P; Zhu, Qingwen Q; Dong, Wenrong W; Zhang, Siqi S; Sun, Yanyan Y; Du, Xitong X; Geng, Meng M; Jiang, Yuan Y
Publication Date: 2022

Variant appearance in text: rs7097
PubMed Link: 36350814
Variant Present in the following documents:
  • pone.0276233.s004.xlsx, sheet 1
View BVdb publication page



Beneficial effects of mifepristone treatment in breast cancer patients selected by the progesterone receptor isoform ratio: Results from the MIPRA trial.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Elía, Andrés A; Saldain, Leo L; Vanzulli, Silvia I SI; Helguero, Luisa A LA; Lamb, Caroline A CA; Fabris, Victoria V; Pataccini, Gabriela G; Martínez-Vazquez, Paula P; Burruchaga, Javier J; Caillet-Bois, Ines I; Spengler, Eunice E; Acosta Haab, Gabriela G; Liguori, Marcos M; Castets, Alejandra A; Lovisi, Silvia S; Abascal, María F MF; Novaro, Virginia V; Sánchez, Jana J; Muñoz, Javier J; Belizán, Jose M JM; Abba, Martín C MC; Gass, Hugo H; Rojas, Paola P; Lanari, Claudia C
Publication Date: 2022-10-21

Variant appearance in text: rs7097
PubMed Link: 36269797
Variant Present in the following documents:
  • ccr-22-2060_supplementary_table_s5_suppts5.xlsx, sheet 1
View BVdb publication page



Next-generation whole exome sequencing to delineate the genetic basis of primary congenital glaucoma.

Scientific Reports
Rauf, Bushra B; Khan, Shahid Y SY; Jiao, Xiaodong X; Irum, Bushra B; Ashfaq, Ramla R; Zehra, Mubashra M; Khan, Asma A AA; Naeem, Muhammad Asif MA; Shahzad, Mohsin M; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-10-14

Variant appearance in text: rs7097
PubMed Link: 36241656
Variant Present in the following documents:
  • 41598_2022_20939_MOESM14_ESM.xlsx, sheet 2
View BVdb publication page



A genomic deletion encompassing CRYBB2-CRYBB2P1 is responsible for autosomal recessive congenital cataracts.

Human Genome Variation
Irum, Bushra B; Kabir, Firoz F; Shoshany, Nadav N; Khan, Shahid Y SY; Rauf, Bushra B; Naeem, Muhammad Asif MA; Qaiser, Tanveer A TA; Riazuddin, Sheikh S; Hejtmancik, J Fielding JF; Riazuddin, S Amer SA
Publication Date: 2022-09-08

Variant appearance in text: rs7097
PubMed Link: 36075891
Variant Present in the following documents:
  • 41439_2022_208_MOESM4_ESM.xlsx, sheet 2
  • 41439_2022_208_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



A novel splice site variant c.1183 + 1 G > C in DFNA5 causing autosomal dominant nonsyndromic hearing loss in a Chinese family.

Bmc Medical Genomics
Li, Qiong Q; Wang, Shujuan S; Liang, Pengfei P; Li, Wei W; Wang, Jian J; Fan, Bei B; Yang, Yang Y; An, Xiaogang X; Chen, Jun J; Zha, Dingjun D
Publication Date: 2022-07-21

Variant appearance in text: rs7097
PubMed Link: 35864542
Variant Present in the following documents:
  • 12920_2022_1315_MOESM2_ESM.xlsx, sheet 3
  • 12920_2022_1315_MOESM2_ESM.xlsx, sheet 1
  • 12920_2022_1315_MOESM3_ESM.xlsx, sheet 2
View BVdb publication page



A novel missense variant in CEACAM16 gene causes autosomal dominant nonsyndromic hearing loss.

Annals Of Human Genetics
Zhang, Dejun D; Wu, Jie J; Yuan, Yongyi Y; Li, Xiaohong X; Gao, Xue X; Han, Mingyu M; Gao, Song S; Huang, Shasha S; Dai, Pu P
Publication Date: 2022-07

Variant appearance in text: rs7097
PubMed Link: 35292975
Variant Present in the following documents:
  • AHG-86-207-s002.xlsx, sheet 1
View BVdb publication page



SNPs in miRNAs and Target Sequences: Role in Cancer and Diabetes.

Frontiers In Genetics
Chhichholiya, Yogita Y; Suryan, Aman Kumar AK; Suman, Prabhat P; Munshi, Anjana A; Singh, Sandeep S
Publication Date: 2021

Variant appearance in text: rs7097
PubMed Link: 34925466
Variant Present in the following documents:
  • Main text
  • fgene-12-793523.pdf
View BVdb publication page



Familial Temperature-Sensitive Auditory Neuropathy: Distinctive Clinical Courses Caused by Variants of the OTOF Gene.

Frontiers In Cell And Developmental Biology
Zhu, Yi-Ming YM; Li, Qi Q; Gao, Xue X; Li, Yan-Fei YF; Liu, You-Li YL; Dai, Pu P; Li, Xiang-Ping XP
Publication Date: 2021

Variant appearance in text: rs7097
PubMed Link: 34692690
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Nuclear Pore Glycoprotein 62 Genetic Variant rs9523 is Associated with Clinical Outcomes of Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitors in Lung Adenocarcinoma Patients.

Pharmacogenomics And Personalized Medicine
Park, Ji Eun JE; Hong, Mi Jeong MJ; Lee, Shin Yup SY; Lee, Jang Hyuck JH; Choi, Jin Eun JE; Kang, Hyo-Gyoung HG; Do, Sook Kyung SK; Jeong, Ji Yun JY; Shin, Kyung Min KM; Lee, Won Kee WK; Choi, Sun Ha SH; Lee, Yong Hoon YH; Seo, Hye Won HW; Yoo, Seung Soo SS; Lee, Jaehee J; Cha, Seung Ick SI; Kim, Chang Ho CH; Park, Jae Yong JY
Publication Date: 2021

Variant appearance in text: rs7097
PubMed Link: 34629889
Variant Present in the following documents:
  • Main text
  • pgpm-14-1291.pdf
View BVdb publication page



Case Report: A Variant Non-ketotic Hyperglycinemia With GLRX5 Mutations: Manifestation of Deficiency of Activities of the Respiratory Chain Enzymes.

Frontiers In Genetics
Feng, Wei-Xing WX; Zhuo, Xiu-Wei XW; Liu, Zhi-Mei ZM; Li, Jiu-Wei JW; Zhang, Wei-Hua WH; Wu, Yun Y; Han, Tong-Li TL; Fang, Fang F
Publication Date: 2021

Variant appearance in text: rs7097
PubMed Link: 34054912
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology
Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA
Publication Date: 2021

Variant appearance in text: rs7097
PubMed Link: 33791233
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Tracking the Genetic Susceptibility Background of B-Cell Non-Hodgkin's Lymphomas from Genome-Wide Association Studies.

International Journal Of Molecular Sciences
Hernández-Verdin, Isaias I; Labreche, Karim K; Benazra, Marion M; Mokhtari, Karima K; Hoang-Xuan, Khê K; Alentorn, Agusti A
Publication Date: 2020-12-24

Variant appearance in text: rs7097
PubMed Link: 33374413
Variant Present in the following documents:
  • Main text
  • ijms-22-00122.pdf
View BVdb publication page



Identification of a nonsense mutation in TNNI3K associated with cardiac conduction disease.

Journal Of Clinical Laboratory Analysis
Liu, Jiang J; Liu, Da D; Li, Muzheng M; Wu, Keke K; Liu, Na N; Zhao, Chenyu C; Shi, Xiaoliu X; Liu, Qiming Q
Publication Date: 2020-09

Variant appearance in text: rs7097
PubMed Link: 32529721
Variant Present in the following documents:
  • JCLA-34-e23418-s003.xls, sheet 1
View BVdb publication page



PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: rs7097
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports
Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA
Publication Date: 2019-10-09

Variant appearance in text: rs7097
PubMed Link: 31597922
Variant Present in the following documents:
  • 41598_2019_50891_MOESM5_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM4_ESM.xlsx, sheet 1
View BVdb publication page



Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases.

Cell Death & Disease
Grassi, Ludovica L; Alfonsi, Romina R; Francescangeli, Federica F; Signore, Michele M; De Angelis, Maria Laura ML; Addario, Antonio A; Costantini, Manuela M; Flex, Elisabetta E; Ciolfi, Andrea A; Pizzi, Simone S; Bruselles, Alessandro A; Pallocca, Matteo M; Simone, Giuseppe G; Haoui, Mustapha M; Falchi, Mario M; Milella, Michele M; Sentinelli, Steno S; Di Matteo, Paola P; Stellacci, Emilia E; Gallucci, Michele M; Muto, Giovanni G; Tartaglia, Marco M; De Maria, Ruggero R; Bonci, Désirée D
Publication Date: 2019-02-27

Variant appearance in text: rs7097
PubMed Link: 30814510
Variant Present in the following documents:
  • 41419_2019_1453_MOESM27_ESM.xlsx, sheet 2
  • 41419_2019_1453_MOESM27_ESM.xlsx, sheet 1
View BVdb publication page



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: POLR1D: 26+1290C>T; rs7097
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_7.xlsx, sheet 1
  • Table_5.xlsx, sheet 1
  • Table_6.xlsx, sheet 1
View BVdb publication page



A likely pathogenic variant putatively affecting splicing of PIGA identified in a multiple congenital anomalies hypotonia-seizures syndrome 2 (MCAHS2) family pedigree via whole-exome sequencing.

Molecular Genetics & Genomic Medicine
Yang, Junli J; Wang, Qiong Q; Zhuo, Qingcui Q; Tian, Huiling H; Li, Wen W; Luo, Fang F; Zhang, Jinghui J; Bi, Dan D; Peng, Jing J; Zhou, Dong D; Xin, Huawei H
Publication Date: 2018-09

Variant appearance in text: rs7097
PubMed Link: 29974678
Variant Present in the following documents:
  • MGG3-6-739-s002.xlsx, sheet 4
  • MGG3-6-739-s002.xlsx, sheet 3
View BVdb publication page



Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation
Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H
Publication Date: 2017

Variant appearance in text: rs7097
PubMed Link: 28690861
Variant Present in the following documents:
  • hgv201727-s1.xls, sheet 1
View BVdb publication page



Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases
Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ
Publication Date: 2017-05-23

Variant appearance in text: rs7097
PubMed Link: 28535796
Variant Present in the following documents:
  • 13023_2017_647_MOESM1_ESM.xlsx, sheet 4
View BVdb publication page



Generation of a High Number of Healthy Erythroid Cells from Gene-Edited Pyruvate Kinase Deficiency Patient-Specific Induced Pluripotent Stem Cells.

Stem Cell Reports
Garate, Zita Z; Quintana-Bustamante, Oscar O; Crane, Ana M AM; Olivier, Emmanuel E; Poirot, Laurent L; Galetto, Roman R; Kosinski, Penelope P; Hill, Collin C; Kung, Charles C; Agirre, Xabi X; Orman, Israel I; Cerrato, Laura L; Alberquilla, Omaira O; Rodriguez-Fornes, Fatima F; Fusaki, Noemi N; Garcia-Sanchez, Felix F; Maia, Tabita M TM; Ribeiro, Maria L ML; Sevilla, Julian J; Prosper, Felipe F; Jin, Shengfang S; Mountford, Joanne J; Guenechea, Guillermo G; Gouble, Agnes A; Bueren, Juan A JA; Davis, Brian R BR; Segovia, Jose C JC
Publication Date: 2015-12-08

Variant appearance in text: rs7097
PubMed Link: 26549847
Variant Present in the following documents:
  • mmc3.xlsx, sheet 3
  • mmc3.xlsx, sheet 1
  • mmc3.xlsx, sheet 2
View BVdb publication page



Tissue-Specific Enrichment of Lymphoma Risk Loci in Regulatory Elements.

Plos One
Hayes, James E JE; Trynka, Gosia G; Vijai, Joseph J; Offit, Kenneth K; Raychaudhuri, Soumya S; Klein, Robert J RJ
Publication Date: 2015

Variant appearance in text: rs7097
PubMed Link: 26422229
Variant Present in the following documents:
  • Main text
  • pone.0139360.pdf
View BVdb publication page



Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach.

Human Genomics
Karageorgos, Ioannis I; Mizzi, Clint C; Giannopoulou, Efstathia E; Pavlidis, Cristiana C; Peters, Brock A BA; Zagoriti, Zoi Z; Stenson, Peter D PD; Mitropoulos, Konstantinos K; Borg, Joseph J; Kalofonos, Haralabos P HP; Drmanac, Radoje R; Stubbs, Andrew A; van der Spek, Peter P; Cooper, David N DN; Katsila, Theodora T; Patrinos, George P GP
Publication Date: 2015-06-20

Variant appearance in text: rs7097
PubMed Link: 26092435
Variant Present in the following documents:
  • 40246_2015_34_MOESM1_ESM.xlsx, sheet 2
View BVdb publication page



Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget
Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S
Publication Date: 2015-06-20

Variant appearance in text: rs7097
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
View BVdb publication page



Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.

Febs Open Bio
Szeto, Carol Ying-Ying CY; Lin, Chi Ho CH; Choi, Siu Chung SC; Yip, Timothy T C TT; Ngan, Roger Kai-Cheong RK; Tsao, George Sai-Wah GS; Li Lung, Maria M
Publication Date: 2014

Variant appearance in text: rs7097
PubMed Link: 24490137
Variant Present in the following documents:
  • mmc5.xlsx, sheet 2
View BVdb publication page



Cis-acting polymorphisms affect complex traits through modifications of microRNA regulation pathways.

Plos One
Arnold, Matthias M; Ellwanger, Daniel C DC; Hartsperger, Mara L ML; Pfeufer, Arne A; Stümpflen, Volker V
Publication Date: 2012

Variant appearance in text: rs7097
PubMed Link: 22606281
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index.

Nature Genetics
Speliotes, Elizabeth K EK; Willer, Cristen J CJ; Berndt, Sonja I SI; Monda, Keri L KL; Thorleifsson, Gudmar G; Jackson, Anne U AU; Lango Allen, Hana H; Lindgren, Cecilia M CM; Luan, Jian'an J; Mägi, Reedik R; Randall, Joshua C JC; Vedantam, Sailaja S; Winkler, Thomas W TW; Qi, Lu L; Workalemahu, Tsegaselassie T; Heid, Iris M IM; Steinthorsdottir, Valgerdur V; Stringham, Heather M HM; Weedon, Michael N MN; Wheeler, Eleanor E; Wood, Andrew R AR; Ferreira, Teresa T; Weyant, Robert J RJ; Segrè, Ayellet V AV; Estrada, Karol K; Liang, Liming L; Nemesh, James J; Park, Ju-Hyun JH; Gustafsson, Stefan S; Kilpeläinen, Tuomas O TO; Yang, Jian J; Bouatia-Naji, Nabila N; Esko, Tõnu T; Feitosa, Mary F MF; Kutalik, Zoltán Z; Mangino, Massimo M; Raychaudhuri, Soumya S; Scherag, Andre A; Smith, Albert Vernon AV; Welch, Ryan R; Zhao, Jing Hua JH; Aben, Katja K KK; Absher, Devin M DM; Amin, Najaf N; Dixon, Anna L AL; Fisher, Eva E; Glazer, Nicole L NL; Goddard, Michael E ME; Heard-Costa, Nancy L NL; Hoesel, Volker V; Hottenga, Jouke-Jan JJ; Johansson, Asa A; Johnson, Toby T; Ketkar, Shamika S; Lamina, Claudia C; Li, Shengxu S; Moffatt, Miriam F MF; Myers, Richard H RH; Narisu, Narisu N; Perry, John R B JR; Peters, Marjolein J MJ; Preuss, Michael M; Ripatti, Samuli S; Rivadeneira, Fernando F; Sandholt, Camilla C; Scott, Laura J LJ; Timpson, Nicholas J NJ; Tyrer, Jonathan P JP; van Wingerden, Sophie S; Watanabe, Richard M RM; White, Charles C CC; Wiklund, Fredrik F; Barlassina, Christina C; Chasman, Daniel I DI; Cooper, Matthew N MN; Jansson, John-Olov JO; Lawrence, Robert W RW; Pellikka, Niina N; Prokopenko, Inga I; Shi, Jianxin J; Thiering, Elisabeth E; Alavere, Helene H; Alibrandi, Maria T S MT; Almgren, Peter P; Arnold, Alice M AM; Aspelund, Thor T; Atwood, Larry D LD; Balkau, Beverley B; Balmforth, Anthony J AJ; Bennett, Amanda J AJ; Ben-Shlomo, Yoav Y; Bergman, Richard N RN; Bergmann, Sven S; Biebermann, Heike H; Blakemore, Alexandra I F AI; Boes, Tanja T; Bonnycastle, Lori L LL; Bornstein, Stefan R SR; Brown, Morris J MJ; Buchanan, Thomas A TA; Busonero, Fabio F; Campbell, Harry H; Cappuccio, Francesco P FP; Cavalcanti-Proença, Christine C; Chen, Yii-Der Ida YD; Chen, Chih-Mei CM; Chines, Peter S PS; Clarke, Robert R; Coin, Lachlan L; Connell, John J; Day, Ian N M IN; den Heijer, Martin M; Duan, Jubao J; Ebrahim, Shah S; Elliott, Paul P; Elosua, Roberto R; Eiriksdottir, Gudny G; Erdos, Michael R MR; Eriksson, Johan G JG; Facheris, Maurizio F MF; Felix, Stephan B SB; Fischer-Posovszky, Pamela P; Folsom, Aaron R AR; Friedrich, Nele N; Freimer, Nelson B NB; Fu, Mao M; Gaget, Stefan S; Gejman, Pablo V PV; Geus, Eco J C EJ; Gieger, Christian C; Gjesing, Anette P AP; Goel, Anuj A; Goyette, Philippe P; Grallert, Harald H; Grässler, Jürgen J; Greenawalt, Danielle M DM; Groves, Christopher J CJ; Gudnason, Vilmundur V; Guiducci, Candace C; Hartikainen, Anna-Liisa AL; Hassanali, Neelam N; Hall, Alistair S AS; Havulinna, Aki S AS; Hayward, Caroline C; Heath, Andrew C AC; Hengstenberg, Christian C; Hicks, Andrew A AA; Hinney, Anke A; Hofman, Albert A; Homuth, Georg G; Hui, Jennie J; Igl, Wilmar W; Iribarren, Carlos C; Isomaa, Bo B; Jacobs, Kevin B KB; Jarick, Ivonne I; Jewell, Elizabeth E; John, Ulrich U; Jørgensen, Torben T; Jousilahti, Pekka P; Jula, Antti A; Kaakinen, Marika M; Kajantie, Eero E; Kaplan, Lee M LM; Kathiresan, Sekar S; Kettunen, Johannes J; Kinnunen, Leena L; Knowles, Joshua W JW; Kolcic, Ivana I; König, Inke R IR; Koskinen, Seppo S; Kovacs, Peter P; Kuusisto, Johanna J; Kraft, Peter P; Kvaløy, Kirsti K; Laitinen, Jaana J; Lantieri, Olivier O; Lanzani, Chiara C; Launer, Lenore J LJ; Lecoeur, Cecile C; Lehtimäki, Terho T; Lettre, Guillaume G; Liu, Jianjun J; Lokki, Marja-Liisa ML; Lorentzon, Mattias M; Luben, Robert N RN; Ludwig, Barbara B; , ; Manunta, Paolo P; Marek, Diana D; Marre, Michel M; Martin, Nicholas G NG; McArdle, Wendy L WL; McCarthy, Anne A; McKnight, Barbara B; Meitinger, Thomas T; Melander, Olle O; Meyre, David D; Midthjell, Kristian K; Montgomery, Grant W GW; Morken, Mario A MA; Morris, Andrew P AP; Mulic, Rosanda R; Ngwa, Julius S JS; Nelis, Mari M; Neville, Matt J MJ; Nyholt, Dale R DR; O'Donnell, Christopher J CJ; O'Rahilly, Stephen S; Ong, Ken K KK; Oostra, Ben B; Paré, Guillaume G; Parker, Alex N AN; Perola, Markus M; Pichler, Irene I; Pietiläinen, Kirsi H KH; Platou, Carl G P CG; Polasek, Ozren O; Pouta, Anneli A; Rafelt, Suzanne S; Raitakari, Olli O; Rayner, Nigel W NW; Ridderstråle, Martin M; Rief, Winfried W; Ruokonen, Aimo A; Robertson, Neil R NR; Rzehak, Peter P; Salomaa, Veikko V; Sanders, Alan R AR; Sandhu, Manjinder S MS; Sanna, Serena S; Saramies, Jouko J; Savolainen, Markku J MJ; Scherag, Susann S; Schipf, Sabine S; Schreiber, Stefan S; Schunkert, Heribert H; Silander, Kaisa K; Sinisalo, Juha J; Siscovick, David S DS; Smit, Jan H JH; Soranzo, Nicole N; Sovio, Ulla U; Stephens, Jonathan J; Surakka, Ida I; Swift, Amy J AJ; Tammesoo, Mari-Liis ML; Tardif, Jean-Claude JC; Teder-Laving, Maris M; Teslovich, Tanya M TM; Thompson, John R JR; Thomson, Brian B; Tönjes, Anke A; Tuomi, Tiinamaija T; van Meurs, Joyce B J JB; van Ommen, Gert-Jan GJ; Vatin, Vincent V; Viikari, Jorma J; Visvikis-Siest, Sophie S; Vitart, Veronique V; Vogel, Carla I G CI; Voight, Benjamin F BF; Waite, Lindsay L LL; Wallaschofski, Henri H; Walters, G Bragi GB; Widen, Elisabeth E; Wiegand, Susanna S; Wild, Sarah H SH; Willemsen, Gonneke G; Witte, Daniel R DR; Witteman, Jacqueline C JC; Xu, Jianfeng J; Zhang, Qunyuan Q; Zgaga, Lina L; Ziegler, Andreas A; Zitting, Paavo P; Beilby, John P JP; Farooqi, I Sadaf IS; Hebebrand, Johannes J; Huikuri, Heikki V HV; James, Alan L AL; Kähönen, Mika M; Levinson, Douglas F DF; Macciardi, Fabio F; Nieminen, Markku S MS; Ohlsson, Claes C; Palmer, Lyle J LJ; Ridker, Paul M PM; Stumvoll, Michael M; Beckmann, Jacques S JS; Boeing, Heiner H; Boerwinkle, Eric E; Boomsma, Dorret I DI; Caulfield, Mark J MJ; Chanock, Stephen J SJ; Collins, Francis S FS; Cupples, L Adrienne LA; Smith, George Davey GD; Erdmann, Jeanette J; Froguel, Philippe P; Grönberg, Henrik H; Gyllensten, Ulf U; Hall, Per P; Hansen, Torben T; Harris, Tamara B TB; Hattersley, Andrew T AT; Hayes, Richard B RB; Heinrich, Joachim J; Hu, Frank B FB; Hveem, Kristian K; Illig, Thomas T; Jarvelin, Marjo-Riitta MR; Kaprio, Jaakko J; Karpe, Fredrik F; Khaw, Kay-Tee KT; Kiemeney, Lambertus A LA; Krude, Heiko H; Laakso, Markku M; Lawlor, Debbie A DA; Metspalu, Andres A; Munroe, Patricia B PB; Ouwehand, Willem H WH; Pedersen, Oluf O; Penninx, Brenda W BW; Peters, Annette A; Pramstaller, Peter P PP; Quertermous, Thomas T; Reinehr, Thomas T; Rissanen, Aila A; Rudan, Igor I; Samani, Nilesh J NJ; Schwarz, Peter E H PE; Shuldiner, Alan R AR; Spector, Timothy D TD; Tuomilehto, Jaakko J; Uda, Manuela M; Uitterlinden, André A; Valle, Timo T TT; Wabitsch, Martin M; Waeber, Gérard G; Wareham, Nicholas J NJ; Watkins, Hugh H; , ; Wilson, James F JF; Wright, Alan F AF; Zillikens, M Carola MC; Chatterjee, Nilanjan N; McCarroll, Steven A SA; Purcell, Shaun S; Schadt, Eric E EE; Visscher, Peter M PM; Assimes, Themistocles L TL; Borecki, Ingrid B IB; Deloukas, Panos P; Fox, Caroline S CS; Groop, Leif C LC; Haritunians, Talin T; Hunter, David J DJ; Kaplan, Robert C RC; Mohlke, Karen L KL; O'Connell, Jeffrey R JR; Peltonen, Leena L; Schlessinger, David D; Strachan, David P DP; van Duijn, Cornelia M CM; Wichmann, H-Erich HE; Frayling, Timothy M TM; Thorsteinsdottir, Unnur U; Abecasis, Gonçalo R GR; Barroso, Inês I; Boehnke, Michael M; Stefansson, Kari K; North, Kari E KE; McCarthy, Mark I MI; Hirschhorn, Joel N JN; Ingelsson, Erik E; Loos, Ruth J F RJ
Publication Date: 2010-11

Variant appearance in text: rs7097
PubMed Link: 20935630
Variant Present in the following documents:
  • NIHMS237282-supplement-1.pdf
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