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rs7164883

From SNPedia

Orientationplus
Stabilizedplus
Make rs7164883(A;A)
Make rs7164883(A;G)
Make rs7164883(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position73359833
GeneHCN4
is asnp
is mentioned by
dbSNPrs7164883
ebirs7164883
HLIrs7164883
Exacrs7164883
Varsomers7164883
Maprs7164883
PheGenIrs7164883
hapmaprs7164883
1000 genomesrs7164883
hgdprs7164883
ensemblrs7164883
gopubmedrs7164883
geneviewrs7164883
scholarrs7164883
googlers7164883
pharmgkbrs7164883
gwascentralrs7164883
openSNPrs7164883
23andMers7164883
23andMe allrs7164883
SNP Nexus

SNPshotrs7164883
SNPdbers7164883
MSV3drs7164883
GWAS Ctlgrs7164883
GMAF0.1882
Max Magnitude
? (A;A) (A;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 G
P-val 3E-17
Odds Ratio 1.1900 None


[PMID 25196315] The rs3807989 G/A Polymorphism in CAV1 is Associated with the Risk of Atrial Fibrillation in Chinese Han Populations