rs13376333

plus

Geno	Mag	Summary
(C;C)	0
(C;T)	1.5	1.5x higher risk of atrial fibrillation
(T;T)	2	~2x higher risk of atrial fibrillation

Reference

GRCh38 38.1/141

Chromosome

1

Position

154841877

Gene

0.2199

2

(C;C) (C;T) (T;T)

28

news atrial fibrillation rs13376333 in KCNN3, with an odds ratio (OR) of 1.5 per copy of rs13376333(T); CI: 1.40–1.64, p = 1.83 × 10e-21.

GWAS snp
PMID	[PMID 20173747 ]
Trait	Atrial fibrillation
Title	Common variants in KCNN3 are associated with lone atrial fibrillation
Risk Allele	T
P-val	2E-21
Odds Ratio	1.52 [1.40-1.64]

[PMID 21107608 ] Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population

[PMID 21760908 ] Association between variants on chromosome 4q25, 16q22 and 1q21 and atrial fibrillation in the Polish population

[PMID 22019810] Significant Association of rs13376333 in KCNN3 on Chromosome 1q21 With Atrial Fibrillation in a Taiwanese Population

[PMID 23428961 ] Common genetic polymorphism at 4q25 locus predicts atrial fibrillation recurrence after successful cardioversion.

[PMID 24978901] Association between SNP rs13376333 and rs1131820 in the KCNN3 gene and atrial fibrillation in the Chinese Han population

[PMID 25684755 ] Common Genetic Variants and Response to Atrial Fibrillation Ablation

[PMID 26370375] KCNN3 SNP rs13376333 on Chromosome 1q21 Confers Increased Risk of Atrial Fibrillation

[PMID 29624624 ] Genetic modulation of atrial fibrillation risk in a Hispanic/Latino cohort.