Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2968857
rs2968857
KCNH2
0.010 GeneticVariation BEFREE We did not observe the association of rs1036145, rs3807375, and rs2968857 with AF. 19490382

2009
dbSNP: rs3807375
rs3807375
KCNH2
0.010 GeneticVariation BEFREE We did not observe the association of rs1036145, rs3807375, and rs2968857 with AF. 19490382

2009
dbSNP: rs2200733
rs2200733 		0.900 GeneticVariation GWASCAT A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. 19597491

2009
dbSNP: rs2200733
rs2200733 		0.900 GeneticVariation GWASDB A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. 19597491

2009
dbSNP: rs7193343
rs7193343
ZFHX3
0.870 GeneticVariation BEFREE A variant in the ZFHX3 gene on chromosome 16q22, rs7193343-T, associated significantly with AF (odds ratio OR = 1.21, P = 1.4 x 10(-10)). 19597491

2009
dbSNP: rs7193343
rs7193343
ZFHX3
T 0.870 GeneticVariation GWASDB A variant in the ZFHX3 gene on chromosome 16q22, rs7193343-T, associated significantly with AF (odds ratio OR = 1.21, P = 1.4 x 10(-10)). 19597491

2009
dbSNP: rs7193343
rs7193343
ZFHX3
T 0.870 GeneticVariation GWASCAT A variant in the ZFHX3 gene on chromosome 16q22, rs7193343-T, associated significantly with AF (odds ratio OR = 1.21, P = 1.4 x 10(-10)). 19597491

2009
dbSNP: rs2220427
rs2220427 		0.800 GeneticVariation GWASDB A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. 19597491

2009
dbSNP: rs2634073
rs2634073 		0.710 GeneticVariation GWASDB A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. 19597491

2009
dbSNP: rs13141190
rs13141190 		0.700 GeneticVariation GWASDB A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. 19597491

2009
dbSNP: rs1448817
rs1448817 		0.700 GeneticVariation GWASDB A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. 19597491

2009
dbSNP: rs16997168
rs16997168 		0.700 GeneticVariation GWASDB A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. 19597491

2009
dbSNP: rs2723316
rs2723316 		0.700 GeneticVariation GWASDB A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke. 19597491

2009
dbSNP: rs2106261
rs2106261
ZFHX3
0.900 GeneticVariation BEFREE 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
dbSNP: rs2106261
rs2106261
ZFHX3
T 0.900 GeneticVariation GWASDB 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
dbSNP: rs2106261
rs2106261
ZFHX3
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
dbSNP: rs17042171
rs17042171 		A 0.810 GeneticVariation GWASDB Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. 19597492

2009
dbSNP: rs17042171
rs17042171 		A 0.810 GeneticVariation GWASCAT Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. 19597492

2009
dbSNP: rs17375901
rs17375901
MTHFR
T 0.800 GeneticVariation GWASCAT Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. 19597492

2009
dbSNP: rs17375901
rs17375901
MTHFR
T 0.800 GeneticVariation GWASDB Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. 19597492

2009
dbSNP: rs17576
rs17576
MMP9
0.010 GeneticVariation BEFREE No relationship between R279Q polymorphism and AF was found in this cohort. 19665460

2009
dbSNP: rs199591851
rs199591851
ACE
0.010 GeneticVariation BEFREE No relationship between R279Q polymorphism and AF was found in this cohort. 19665460

2009
dbSNP: rs2200733
rs2200733 		0.900 GeneticVariation BEFREE Our results suggest that SNP rs2200733 confers a highly significant risk of AF, but not ischemic stroke, in a more representative Chinese Han population in the mainland China. 19707791

2009
dbSNP: rs1352950843
rs1352950843
SCN2B
0.010 GeneticVariation BEFREE We identified 2 nonsynonymous variants in SCN1B (resulting in R85H, D153N) and 2 in SCN2B (R28Q, R28W) in patients with AF. 19808477

2009
dbSNP: rs16969925
rs16969925
SCN1B
0.010 GeneticVariation BEFREE We identified 2 nonsynonymous variants in SCN1B (resulting in R85H, D153N) and 2 in SCN2B (R28Q, R28W) in patients with AF. 19808477

2009