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rs1014922

From SNPedia

Orientationminus
Stabilizedminus
Make rs1014922(A;A)
Make rs1014922(A;C)
Make rs1014922(C;C)
ReferenceGRCh38 38.1/141
Chromosome15
Position94622351
is asnp
is mentioned by
dbSNPrs1014922
ebirs1014922
HLIrs1014922
Exacrs1014922
Varsomers1014922
Maprs1014922
PheGenIrs1014922
hapmaprs1014922
1000 genomesrs1014922
hgdprs1014922
ensemblrs1014922
gopubmedrs1014922
geneviewrs1014922
scholarrs1014922
googlers1014922
pharmgkbrs1014922
gwascentralrs1014922
openSNPrs1014922
23andMers1014922
23andMe allrs1014922
SNP Nexus

SNPshotrs1014922
SNPdbers1014922
MSV3drs1014922
GWAS Ctlgrs1014922
GMAF0.1933
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21658281OA-icon.png]
Trait
Title GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease.
Risk Allele
P-val 0.000003
Odds Ratio 1.3600 [1.20-1.55]