rs2968857
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We did not observe the association of rs1036145, rs3807375, and rs2968857 with AF.
|
19490382 |
2009 |
rs3807375
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We did not observe the association of rs1036145, rs3807375, and rs2968857 with AF.
|
19490382 |
2009 |
rs2200733
|
|
|
0.900 |
GeneticVariation |
GWASCAT |
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
|
19597491 |
2009 |
rs2200733
|
|
|
0.900 |
GeneticVariation |
GWASDB |
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
|
19597491 |
2009 |
rs7193343
|
|
|
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 |
rs7193343
|
|
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 |
rs7193343
|
|
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 |
rs2220427
|
|
|
0.800 |
GeneticVariation |
GWASDB |
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
|
19597491 |
2009 |
rs2634073
|
|
|
0.710 |
GeneticVariation |
GWASDB |
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
|
19597491 |
2009 |
rs13141190
|
|
|
0.700 |
GeneticVariation |
GWASDB |
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
|
19597491 |
2009 |
rs1448817
|
|
|
0.700 |
GeneticVariation |
GWASDB |
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
|
19597491 |
2009 |
rs16997168
|
|
|
0.700 |
GeneticVariation |
GWASDB |
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
|
19597491 |
2009 |
rs2723316
|
|
|
0.700 |
GeneticVariation |
GWASDB |
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
|
19597491 |
2009 |
rs2106261
|
|
|
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 |
rs2106261
|
|
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 |
rs2106261
|
|
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 |
rs17042171
|
|
A |
0.810 |
GeneticVariation |
GWASDB |
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.
|
19597492 |
2009 |
rs17042171
|
|
A |
0.810 |
GeneticVariation |
GWASCAT |
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.
|
19597492 |
2009 |
rs17375901
|
|
T |
0.800 |
GeneticVariation |
GWASCAT |
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.
|
19597492 |
2009 |
rs17375901
|
|
T |
0.800 |
GeneticVariation |
GWASDB |
Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.
|
19597492 |
2009 |
rs17576
|
|
|
0.010 |
GeneticVariation |
BEFREE |
No relationship between R279Q polymorphism and AF was found in this cohort.
|
19665460 |
2009 |
rs199591851
|
|
|
0.010 |
GeneticVariation |
BEFREE |
No relationship between R279Q polymorphism and AF was found in this cohort.
|
19665460 |
2009 |
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 |
rs1352950843
|
|
|
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 |
rs16969925
|
|
|
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 |