KCNK5 c.187-11159A>G

Variant ID: 6-39174922-T-C

NM_003740.3(KCNK5):c.187-11159A>G

This variant was identified in 30 publications

View GRCh38 version.




Publications:


Polygenic risk for coronary artery disease in the Scottish and English population.

Bmc Cardiovascular Disorders
Yang, Chuhua C; Starnecker, Fabian F; Pang, Shichao S; Chen, Zhifen Z; Güldener, Ulrich U; Li, Ling L; Heinig, Matthias M; Schunkert, Heribert H
Publication Date: 2021-12-07

Variant appearance in text: rs10947789
PubMed Link: 34876023
Variant Present in the following documents:
  • 12872_2021_2398_MOESM1_ESM.pdf
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Cardiovascular risk factor mediation of the effects of education and Genetic Risk Score on cardiovascular disease: a prospective observational cohort study of the Framingham Heart Study.

Bmj Open
Powell, Katie L KL; Stephens, Sebastien R SR; Stephens, Alexandre S AS
Publication Date: 2021-01-12

Variant appearance in text: rs10947789
PubMed Link: 33436477
Variant Present in the following documents:
  • bmjopen-2020-045210.draft_revisions.pdf
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Genetic Risk Score for Coronary Heart Disease: Review.

Journal Of Personalized Medicine
Semaev, Sergey S; Shakhtshneider, Elena E
Publication Date: 2020-11-20

Variant appearance in text: rs10947789
PubMed Link: 33233501
Variant Present in the following documents:
  • Main text
  • jpm-10-00239.pdf
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Prioritization of causal genes for coronary artery disease based on cumulative evidence from experimental and in silico studies.

Scientific Reports
Shadrina, Alexandra S AS; Shashkova, Tatiana I TI; Torgasheva, Anna A AA; Sharapov, Sodbo Z SZ; Klarić, Lucija L; Pakhomov, Eugene D ED; Alexeev, Dmitry G DG; Wilson, James F JF; Tsepilov, Yakov A YA; Joshi, Peter K PK; Aulchenko, Yurii S YS
Publication Date: 2020-06-26

Variant appearance in text: rs10947789
PubMed Link: 32591598
Variant Present in the following documents:
  • Main text
  • 41598_2020_67001_MOESM6_ESM.pdf
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Precision Medicine and Cardiovascular Health: Insights from Mendelian Randomization Analyses.

Korean Circulation Journal
Spiller, Wes W; Jung, Keum Ji KJ; Lee, Ji Young JY; Jee, Sun Ha SH
Publication Date: 2020-02

Variant appearance in text: rs10947789
PubMed Link: 31845553
Variant Present in the following documents:
  • Main text
  • kcj-50-91.pdf
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A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria.

Diabetologia
Ahluwalia, Tarunveer S TS; Schulz, Christina-Alexandra CA; Waage, Johannes J; Skaaby, Tea T; Sandholm, Niina N; van Zuydam, Natalie N; Charmet, Romain R; Bork-Jensen, Jette J; Almgren, Peter P; Thuesen, Betina H BH; Bedin, Mathilda M; Brandslund, Ivan I; Christensen, Cramer K CK; Linneberg, Allan A; Ahlqvist, Emma E; Groop, Per-Henrik PH; Hadjadj, Samy S; Tregouet, David-Alexandre DA; Jørgensen, Marit E ME; Grarup, Niels N; Pedersen, Oluf O; Simons, Matias M; Groop, Leif L; Orho-Melander, Marju M; McCarthy, Mark I MI; Melander, Olle O; Rossing, Peter P; Kilpeläinen, Tuomas O TO; Hansen, Torben T
Publication Date: 2019-02

Variant appearance in text: rs10947789
PubMed Link: 30547231
Variant Present in the following documents:
  • Main text
  • 125_2018_4783_MOESM1_ESM.pdf
  • 125_2018_Article_4783.pdf
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Genome-wide association study of coronary artery disease among individuals with diabetes: the UK Biobank.

Diabetologia
Fall, Tove T; Gustafsson, Stefan S; Orho-Melander, Marju M; Ingelsson, Erik E
Publication Date: 2018-10

Variant appearance in text: rs10947789
PubMed Link: 30003307
Variant Present in the following documents:
  • 125_2018_4686_MOESM1_ESM.pdf
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Polygenic Risk Score for Coronary Heart Disease Modifies the Elevated Risk by Cigarette Smoking for Disease Incidence.

Circulation. Genomic And Precision Medicine
Hindy, George G; Wiberg, Frans F; Almgren, Peter P; Melander, Olle O; Orho-Melander, Marju M
Publication Date: 2018-01

Variant appearance in text: rs10947789
PubMed Link: 29874179
Variant Present in the following documents:
  • hcg-11-e001856-s001.pdf
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Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes.

Cardiovascular Diabetology
Charmet, Romain R; Duffy, Seamus S; Keshavarzi, Sareh S; Gyorgy, Beata B; Marre, Michel M; Rossing, Peter P; McKnight, Amy Jayne AJ; Maxwell, Alexander P AP; Ahluwalia, Tarun Veer Singh TVS; Paterson, Andrew D AD; Trégouët, David-Alexandre DA; Hadjadj, Samy S
Publication Date: 2018-04-25

Variant appearance in text: rs10947789
PubMed Link: 29695241
Variant Present in the following documents:
  • Main text
  • 12933_2018_Article_705.pdf
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Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease.

Circulation Research
van der Harst, Pim P; Verweij, Niek N
Publication Date: 2018-02-02

Variant appearance in text: rs10947789
PubMed Link: 29212778
Variant Present in the following documents:
  • Main text
  • res-122-433.pdf
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Coronary artery disease-associated genetic variants and biomarkers of inflammation.

Plos One
Christiansen, Morten Krogh MK; Larsen, Sanne Bøjet SB; Nyegaard, Mette M; Neergaard-Petersen, Søs S; Ajjan, Ramzi R; Würtz, Morten M; Grove, Erik Lerkevang EL; Hvas, Anne-Mette AM; Jensen, Henrik Kjærulf HK; Kristensen, Steen Dalby SD
Publication Date: 2017

Variant appearance in text: rs10947789
PubMed Link: 28686695
Variant Present in the following documents:
  • Main text
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Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy.

Plos Genetics
Byars, Sean G SG; Huang, Qin Qin QQ; Gray, Lesley-Ann LA; Bakshi, Andrew A; Ripatti, Samuli S; Abraham, Gad G; Stearns, Stephen C SC; Inouye, Michael M
Publication Date: 2017-06

Variant appearance in text: rs10947789
PubMed Link: 28640878
Variant Present in the following documents:
  • pgen.1006328.s006.pdf
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Heart Disease and Stroke Statistics-2017 Update: A Report From the American Heart Association.

Circulation
Benjamin, Emelia J EJ; Blaha, Michael J MJ; Chiuve, Stephanie E SE; Cushman, Mary M; Das, Sandeep R SR; Deo, Rajat R; de Ferranti, Sarah D SD; Floyd, James J; Fornage, Myriam M; Gillespie, Cathleen C; Isasi, Carmen R CR; Jiménez, Monik C MC; Jordan, Lori Chaffin LC; Judd, Suzanne E SE; Lackland, Daniel D; Lichtman, Judith H JH; Lisabeth, Lynda L; Liu, Simin S; Longenecker, Chris T CT; Mackey, Rachel H RH; Matsushita, Kunihiro K; Mozaffarian, Dariush D; Mussolino, Michael E ME; Nasir, Khurram K; Neumar, Robert W RW; Palaniappan, Latha L; Pandey, Dilip K DK; Thiagarajan, Ravi R RR; Reeves, Mathew J MJ; Ritchey, Matthew M; Rodriguez, Carlos J CJ; Roth, Gregory A GA; Rosamond, Wayne D WD; Sasson, Comilla C; Towfighi, Amytis A; Tsao, Connie W CW; Turner, Melanie B MB; Virani, Salim S SS; Voeks, Jenifer H JH; Willey, Joshua Z JZ; Wilkins, John T JT; Wu, Jason Hy JH; Alger, Heather M HM; Wong, Sally S SS; Muntner, Paul P; ,
Publication Date: 2017-03-07

Variant appearance in text: rs10947789
PubMed Link: 28122885
Variant Present in the following documents:
  • Main text
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Coronary Artery Calcification and Rheumatoid Arthritis: Lack of Relationship to Risk Alleles for Coronary Artery Disease in the General Population.

Arthritis & Rheumatology (Hoboken, N.J.)
Ferraz-Amaro, Iván I; Winchester, Robert R; Gregersen, Peter K PK; Reynolds, Richard J RJ; Wasko, Mary Chester MC; Oeser, Anette A; Chung, Cecilia P CP; Stein, C Michael CM; Giles, Jon T JT; Bathon, Joan M JM
Publication Date: 2017-03

Variant appearance in text: rs10947789
PubMed Link: 27696788
Variant Present in the following documents:
  • Main text
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The impact of genome-wide association studies on the pathophysiology and therapy of cardiovascular disease.

Embo Molecular Medicine
Kessler, Thorsten T; Vilne, Baiba B; Schunkert, Heribert H
Publication Date: 2016-07

Variant appearance in text: rs10947789
PubMed Link: 27189168
Variant Present in the following documents:
  • Main text
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Detailed analysis of association between common single nucleotide polymorphisms and subclinical atherosclerosis: The Multi-ethnic Study of Atherosclerosis.

Data In Brief
Vargas, Jose D JD; Manichaikul, Ani A; Wang, Xin-Qun XQ; Rich, Stephen S SS; Rotter, Jerome I JI; Post, Wendy S WS; Polak, Joseph F JF; Budoff, Matthew J MJ; Bluemke, David A DA
Publication Date: 2016-06

Variant appearance in text: rs10947789
PubMed Link: 26958643
Variant Present in the following documents:
  • Main text
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Genome-Wide Association Study for Incident Myocardial Infarction and Coronary Heart Disease in Prospective Cohort Studies: The CHARGE Consortium.

Plos One
Dehghan, Abbas A; Bis, Joshua C JC; White, Charles C CC; Smith, Albert Vernon AV; Morrison, Alanna C AC; Cupples, L Adrienne LA; Trompet, Stella S; Chasman, Daniel I DI; Lumley, Thomas T; Völker, Uwe U; Buckley, Brendan M BM; Ding, Jingzhong J; Jensen, Majken K MK; Folsom, Aaron R AR; Kritchevsky, Stephen B SB; Girman, Cynthia J CJ; Ford, Ian I; Dörr, Marcus M; Salomaa, Veikko V; Uitterlinden, André G AG; Eiriksdottir, Gudny G; Vasan, Ramachandran S RS; Franceschini, Nora N; Carty, Cara L CL; Virtamo, Jarmo J; Demissie, Serkalem S; Amouyel, Philippe P; Arveiler, Dominique D; Heckbert, Susan R SR; Ferrières, Jean J; Ducimetière, Pierre P; Smith, Nicholas L NL; Wang, Ying A YA; Siscovick, David S DS; Rice, Kenneth M KM; Wiklund, Per-Gunnar PG; Taylor, Kent D KD; Evans, Alun A; Kee, Frank F; Rotter, Jerome I JI; Karvanen, Juha J; Kuulasmaa, Kari K; Heiss, Gerardo G; Kraft, Peter P; Launer, Lenore J LJ; Hofman, Albert A; Markus, Marcello R P MR; Rose, Lynda M LM; Silander, Kaisa K; Wagner, Peter P; Benjamin, Emelia J EJ; Lohman, Kurt K; Stott, David J DJ; Rivadeneira, Fernando F; Harris, Tamara B TB; Levy, Daniel D; Liu, Yongmei Y; Rimm, Eric B EB; Jukema, J Wouter JW; Völzke, Henry H; Ridker, Paul M PM; Blankenberg, Stefan S; Franco, Oscar H OH; Gudnason, Vilmundur V; Psaty, Bruce M BM; Boerwinkle, Eric E; O'Donnell, Christopher J CJ
Publication Date: 2016

Variant appearance in text: rs10947789
PubMed Link: 26950853
Variant Present in the following documents:
  • Main text
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From Loci to Biology: Functional Genomics of Genome-Wide Association for Coronary Disease.

Circulation Research
Nurnberg, Sylvia T ST; Zhang, Hanrui H; Hand, Nicholas J NJ; Bauer, Robert C RC; Saleheen, Danish D; Reilly, Muredach P MP; Rader, Daniel J DJ
Publication Date: 2016-02-19

Variant appearance in text: rs10947789
PubMed Link: 26892960
Variant Present in the following documents:
  • Main text
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Experimental Biology for the Identification of Causal Pathways in Atherosclerosis.

Cardiovascular Drugs And Therapy
Guo, Yanhong Y; Garcia-Barrio, Minerva T MT; Wang, Laiyuan L; Chen, Y Eugene YE
Publication Date: 2016-02

Variant appearance in text: rs10947789
PubMed Link: 26847647
Variant Present in the following documents:
  • Main text
  • 10557_2016_Article_6644.pdf
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Genome-wide association studies of late-onset cardiovascular disease.

Journal Of Molecular And Cellular Cardiology
Smith, J Gustav JG; Newton-Cheh, Christopher C
Publication Date: 2015-06

Variant appearance in text: rs10947789
PubMed Link: 25870159
Variant Present in the following documents:
  • Main text
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GWAS-identified loci for coronary heart disease are associated with intima-media thickness and plaque presence at the carotid artery bulb.

Atherosclerosis
den Hoed, Marcel M; Strawbridge, Rona J RJ; Almgren, Peter P; Gustafsson, Stefan S; Axelsson, Tomas T; Engström, Gunnar G; de Faire, Ulf U; Hedblad, Bo B; Humphries, Steve E SE; Lindgren, Cecilia M CM; Morris, Andrew P AP; Östling, Gerd G; Syvänen, Ann-Christine AC; Tremoli, Elena E; Hamsten, Anders A; Ingelsson, Erik E; Melander, Olle O; Lind, Lars L
Publication Date: 2015-04

Variant appearance in text: rs10947789
PubMed Link: 25682028
Variant Present in the following documents:
  • Main text
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Prospective associations of coronary heart disease loci in African Americans using the MetaboChip: the PAGE study.

Plos One
Franceschini, Nora N; Hu, Yijuan Y; Reiner, Alex P AP; Buyske, Steven S; Nalls, Mike M; Yanek, Lisa R LR; Li, Yun Y; Hindorff, Lucia A LA; Cole, Shelley A SA; Howard, Barbara V BV; Stafford, Jeanette M JM; Carty, Cara L CL; Sethupathy, Praveen P; Martin, Lisa W LW; Lin, Dan-Yu DY; Johnson, Karen C KC; Becker, Lewis C LC; North, Kari E KE; Dehghan, Abbas A; Bis, Joshua C JC; Liu, Yongmei Y; Greenland, Philip P; Manson, JoAnn E JE; Maeda, Nobuyo N; Garcia, Melissa M; Harris, Tamara B TB; Becker, Diane M DM; O'Donnell, Christopher C; Heiss, Gerardo G; Kooperberg, Charles C; Boerwinkle, Eric E
Publication Date: 2014

Variant appearance in text: rs10947789
PubMed Link: 25542012
Variant Present in the following documents:
  • Main text
  • pone.0113203.pdf
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Genetics of coronary artery disease: an update.

Methodist Debakey Cardiovascular Journal
Roberts, Robert R
Publication Date: 2014

Variant appearance in text: rs10947789
PubMed Link: 24932356
Variant Present in the following documents:
  • Main text
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Current Insights into the Joint Genetic Basis of Type 2 Diabetes and Coronary Heart Disease.

Current Cardiovascular Risk Reports
Dauriz, Marco M; Meigs, James B JB
Publication Date: 2014-01-01

Variant appearance in text: rs10947789
PubMed Link: 24729826
Variant Present in the following documents:
  • Main text
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Pathogenesis of coronary artery disease: focus on genetic risk factors and identification of genetic variants.

The Application Of Clinical Genetics
Sayols-Baixeras, Sergi S; Lluís-Ganella, Carla C; Lucas, Gavin G; Elosua, Roberto R
Publication Date: 2014

Variant appearance in text: rs10947789
PubMed Link: 24520200
Variant Present in the following documents:
  • Main text
  • tacg-7-015.pdf
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Heart disease and stroke statistics--2014 update: a report from the American Heart Association.

Circulation
Go, Alan S AS; Mozaffarian, Dariush D; Roger, Véronique L VL; Benjamin, Emelia J EJ; Berry, Jarett D JD; Blaha, Michael J MJ; Dai, Shifan S; Ford, Earl S ES; Fox, Caroline S CS; Franco, Sheila S; Fullerton, Heather J HJ; Gillespie, Cathleen C; Hailpern, Susan M SM; Heit, John A JA; Howard, Virginia J VJ; Huffman, Mark D MD; Judd, Suzanne E SE; Kissela, Brett M BM; Kittner, Steven J SJ; Lackland, Daniel T DT; Lichtman, Judith H JH; Lisabeth, Lynda D LD; Mackey, Rachel H RH; Magid, David J DJ; Marcus, Gregory M GM; Marelli, Ariane A; Matchar, David B DB; McGuire, Darren K DK; Mohler, Emile R ER; Moy, Claudia S CS; Mussolino, Michael E ME; Neumar, Robert W RW; Nichol, Graham G; Pandey, Dilip K DK; Paynter, Nina P NP; Reeves, Matthew J MJ; Sorlie, Paul D PD; Stein, Joel J; Towfighi, Amytis A; Turan, Tanya N TN; Virani, Salim S SS; Wong, Nathan D ND; Woo, Daniel D; Turner, Melanie B MB; ,
Publication Date: 2014-01-21

Variant appearance in text: rs10947789
PubMed Link: 24352519
Variant Present in the following documents:
  • Main text
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Common genetic variants do not associate with CAD in familial hypercholesterolemia.

European Journal Of Human Genetics : Ejhg
van Iperen, Erik P A EP; Sivapalaratnam, Suthesh S; Boekholdt, S Matthijs SM; Hovingh, G Kees GK; Maiwald, Stephanie S; Tanck, Michael W MW; Soranzo, Nicole N; Stephens, Jonathan C JC; Sambrook, Jennifer G JG; Levi, Marcel M; Ouwehand, Willem H WH; Kastelein, John Jp JJ; Trip, Mieke D MD; Zwinderman, Aeilko H AH
Publication Date: 2014-06

Variant appearance in text: rs10947789
PubMed Link: 24219970
Variant Present in the following documents:
  • Main text
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From genotype to phenotype in human atherosclerosis--recent findings.

Current Opinion In Lipidology
Holdt, Lesca M LM; Teupser, Daniel D
Publication Date: 2013-10

Variant appearance in text: rs10947789
PubMed Link: 24005217
Variant Present in the following documents:
  • colip-24-410.pdf
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Genetics of coronary artery disease.

Circulation
Lieb, Wolfgang W; Vasan, Ramachandran S RS
Publication Date: 2013-09-03

Variant appearance in text: rs10947789
PubMed Link: 24002717
Variant Present in the following documents:
  • Main text
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Large-scale association analysis identifies new risk loci for coronary artery disease.

Nature Genetics
, ; Deloukas, Panos P; Kanoni, Stavroula S; Willenborg, Christina C; Farrall, Martin M; Assimes, Themistocles L TL; Thompson, John R JR; Ingelsson, Erik E; Saleheen, Danish D; Erdmann, Jeanette J; Goldstein, Benjamin A BA; Stirrups, Kathleen K; König, Inke R IR; Cazier, Jean-Baptiste JB; Johansson, Asa A; Hall, Alistair S AS; Lee, Jong-Young JY; Willer, Cristen J CJ; Chambers, John C JC; Esko, Tõnu T; Folkersen, Lasse L; Goel, Anuj A; Grundberg, Elin E; Havulinna, Aki S AS; Ho, Weang K WK; Hopewell, Jemma C JC; Eriksson, Niclas N; Kleber, Marcus E ME; Kristiansson, Kati K; Lundmark, Per P; Lyytikäinen, Leo-Pekka LP; Rafelt, Suzanne S; Shungin, Dmitry D; Strawbridge, Rona J RJ; Thorleifsson, Gudmar G; Tikkanen, Emmi E; Van Zuydam, Natalie N; Voight, Benjamin F BF; Waite, Lindsay L LL; Zhang, Weihua W; Ziegler, Andreas A; Absher, Devin D; Altshuler, David D; Balmforth, Anthony J AJ; Barroso, Inês I; Braund, Peter S PS; Burgdorf, Christof C; Claudi-Boehm, Simone S; Cox, David D; Dimitriou, Maria M; Do, Ron R; , ; , ; Doney, Alex S F AS; El Mokhtari, NourEddine N; Eriksson, Per P; Fischer, Krista K; Fontanillas, Pierre P; Franco-Cereceda, Anders A; Gigante, Bruna B; Groop, Leif L; Gustafsson, Stefan S; Hager, Jörg J; Hallmans, Göran G; Han, Bok-Ghee BG; Hunt, Sarah E SE; Kang, Hyun M HM; Illig, Thomas T; Kessler, Thorsten T; Knowles, Joshua W JW; Kolovou, Genovefa G; Kuusisto, Johanna J; Langenberg, Claudia C; Langford, Cordelia C; Leander, Karin K; Lokki, Marja-Liisa ML; Lundmark, Anders A; McCarthy, Mark I MI; Meisinger, Christa C; Melander, Olle O; Mihailov, Evelin E; Maouche, Seraya S; Morris, Andrew D AD; Müller-Nurasyid, Martina M; , ; Nikus, Kjell K; Peden, John F JF; Rayner, N William NW; Rasheed, Asif A; Rosinger, Silke S; Rubin, Diana D; Rumpf, Moritz P MP; Schäfer, Arne A; Sivananthan, Mohan M; Song, Ci C; Stewart, Alexandre F R AF; Tan, Sian-Tsung ST; Thorgeirsson, Gudmundur G; van der Schoot, C Ellen CE; Wagner, Peter J PJ; , ; Wells, George A GA; Wild, Philipp S PS; Yang, Tsun-Po TP; Amouyel, Philippe P; Arveiler, Dominique D; Basart, Hanneke H; Boehnke, Michael M; Boerwinkle, Eric E; Brambilla, Paolo P; Cambien, Francois F; Cupples, Adrienne L AL; de Faire, Ulf U; Dehghan, Abbas A; Diemert, Patrick P; Epstein, Stephen E SE; Evans, Alun A; Ferrario, Marco M MM; Ferrières, Jean J; Gauguier, Dominique D; Go, Alan S AS; Goodall, Alison H AH; Gudnason, Villi V; Hazen, Stanley L SL; Holm, Hilma H; Iribarren, Carlos C; Jang, Yangsoo Y; Kähönen, Mika M; Kee, Frank F; Kim, Hyo-Soo HS; Klopp, Norman N; Koenig, Wolfgang W; Kratzer, Wolfgang W; Kuulasmaa, Kari K; Laakso, Markku M; Laaksonen, Reijo R; Lee, Ji-Young JY; Lind, Lars L; Ouwehand, Willem H WH; Parish, Sarah S; Park, Jeong E JE; Pedersen, Nancy L NL; Peters, Annette A; Quertermous, Thomas T; Rader, Daniel J DJ; Salomaa, Veikko V; Schadt, Eric E; Shah, Svati H SH; Sinisalo, Juha J; Stark, Klaus K; Stefansson, Kari K; Trégouët, David-Alexandre DA; Virtamo, Jarmo J; Wallentin, Lars L; Wareham, Nicholas N; Zimmermann, Martina E ME; Nieminen, Markku S MS; Hengstenberg, Christian C; Sandhu, Manjinder S MS; Pastinen, Tomi T; Syvänen, Ann-Christine AC; Hovingh, G Kees GK; Dedoussis, George G; Franks, Paul W PW; Lehtimäki, Terho T; Metspalu, Andres A; Zalloua, Pierre A PA; Siegbahn, Agneta A; Schreiber, Stefan S; Ripatti, Samuli S; Blankenberg, Stefan S SS; Perola, Markus M; Clarke, Robert R; Boehm, Bernhard O BO; O'Donnell, Christopher C; Reilly, Muredach P MP; März, Winfried W; Collins, Rory R; Kathiresan, Sekar S; Hamsten, Anders A; Kooner, Jaspal S JS; Thorsteinsdottir, Unnur U; Danesh, John J; Palmer, Colin N A CN; Roberts, Robert R; Watkins, Hugh H; Schunkert, Heribert H; Samani, Nilesh J NJ
Publication Date: 2013-01

Variant appearance in text: rs10947789
PubMed Link: 23202125
Variant Present in the following documents:
  • Main text
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