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rs3864663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs3864663(C;C)
Make rs3864663(C;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position77768114
is asnp
is mentioned by
dbSNPrs3864663
ebirs3864663
HLIrs3864663
Exacrs3864663
Varsomers3864663
Maprs3864663
PheGenIrs3864663
hapmaprs3864663
1000 genomesrs3864663
hgdprs3864663
ensemblrs3864663
gopubmedrs3864663
geneviewrs3864663
scholarrs3864663
googlers3864663
pharmgkbrs3864663
gwascentralrs3864663
openSNPrs3864663
23andMers3864663
23andMe allrs3864663
SNP Nexus

SNPshotrs3864663
SNPdbers3864663
MSV3drs3864663
GWAS Ctlgrs3864663
GMAF0.05464
Max Magnitude0
? (C;C) (C;T) (T;T) 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 0.000002
Odds Ratio 1.4000 [1.22-1.61]