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rs5762311

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs5762311(A;A)
Make rs5762311(A;G)
ReferenceGRCh38 38.1/141
Chromosome22
Position27694209
is asnp
is mentioned by
dbSNPrs5762311
ebirs5762311
HLIrs5762311
Exacrs5762311
Varsomers5762311
Maprs5762311
PheGenIrs5762311
hapmaprs5762311
1000 genomesrs5762311
hgdprs5762311
ensemblrs5762311
gopubmedrs5762311
geneviewrs5762311
scholarrs5762311
googlers5762311
pharmgkbrs5762311
gwascentralrs5762311
openSNPrs5762311
23andMers5762311
23andMe allrs5762311
SNP Nexus

SNPshotrs5762311
SNPdbers5762311
MSV3drs5762311
GWAS Ctlgrs5762311
GMAF0.2897
Max Magnitude0
? (A;A) (A;G) (G;G) 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 0.000007
Odds Ratio 2.0300 [1.49-2.75]