Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6843082
rs6843082 		G 0.810 GeneticVariation GWASCAT Multi-ethnic genome-wide association study for atrial fibrillation. 29892015

2018
dbSNP: rs6843082
rs6843082 		G 0.810 GeneticVariation GWASCAT Identification of six new genetic loci associated with atrial fibrillation in the Japanese population. 28416822

2017
dbSNP: rs6843082
rs6843082 		G 0.810 GeneticVariation GWASCAT Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. 28416818

2017
dbSNP: rs6843082
rs6843082 		0.810 GeneticVariation BEFREE The SNPs at the PITX2 and ZFHX3 loci, but not the KCNN3 locus, were significantly associated with AF (PITX2/rs6843082_G: odds ratio 3.41, 95% CI 2.55 to 4.55, P=1.32×10(-16); PITX2/rs2200733_T: odds ratio 2.05, 95% CI 1.66 to 2.53, P=2.20×10(-11); ZFHX3/rs2106261_A: odds ratio 2.33, 95% CI 1.87 to 2.91, P=3.75×10(-14); KCNN3/rs13376333_T: odds ratio 1.74, 95% CI 0.93 to 3.25, P=0.085). 26272656

2015
dbSNP: rs6843082
rs6843082 		G 0.810 GeneticVariation GWASCAT Common variants in KCNN3 are associated with lone atrial fibrillation. 20173747

2010
dbSNP: rs6843082
rs6843082 		G 0.810 GeneticVariation GWASDB Common variants in KCNN3 are associated with lone atrial fibrillation. 20173747

2010