Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2106261
rs2106261
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
T 0.900 GeneticVariation GWASCAT Korean atrial fibrillation network genome-wide association study for early-onset atrial fibrillation identifies novel susceptibility loci. 28460022

2017

dbSNP: rs2106261
rs2106261
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
T 0.900 GeneticVariation GWASCAT Identification of six new genetic loci associated with atrial fibrillation in the Japanese population. 28416822

2017

dbSNP: rs2106261
rs2106261
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
T 0.900 GeneticVariation GWASCAT Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. 28416818

2017

dbSNP: rs2106261
rs2106261
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
T 0.900 GeneticVariation GWASCAT Meta-analysis identifies six new susceptibility loci for atrial fibrillation. 22544366

2012

dbSNP: rs2106261
rs2106261
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation
T 0.900 GeneticVariation GWASCAT Meta-analyses of 896 prevalent (15,768 referents) and 2,517 incident (21,337 referents) AF cases identified a new locus for AF (ZFHX3, rs2106261, risk ratio RR = 1.19; P = 2.3 x 10(-7)). 19597492

2009