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rs6666258

From SNPedia

Orientationplus
Stabilizedplus
Make rs6666258(C;C)
Make rs6666258(C;G)
Make rs6666258(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position154841792
GeneKCNN3
is asnp
is mentioned by
dbSNPrs6666258
ebirs6666258
HLIrs6666258
Exacrs6666258
Varsomers6666258
Maprs6666258
PheGenIrs6666258
hapmaprs6666258
1000 genomesrs6666258
hgdprs6666258
ensemblrs6666258
gopubmedrs6666258
geneviewrs6666258
scholarrs6666258
googlers6666258
pharmgkbrs6666258
gwascentralrs6666258
openSNPrs6666258
23andMers6666258
23andMe allrs6666258
SNP Nexus

SNPshotrs6666258
SNPdbers6666258
MSV3drs6666258
GWAS Ctlgrs6666258
GMAF0.2479
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 22544366OA-icon.png]
Trait
Title Meta-analysis identifies six new susceptibility loci for atrial fibrillation.
Risk Allele C
P-val 2E-14
Odds Ratio 1.1800 None

[PMID 27179719] Impact of genetic variants on the upstream efficacy of renin-angiotensin system inhibitors for the prevention of atrial fibrillation.