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rs10777317

From SNPedia

Orientationplus
Stabilizedplus
Make rs10777317(C;C)
Make rs10777317(C;T)
Make rs10777317(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position91586597
is asnp
is mentioned by
dbSNPrs10777317
ebirs10777317
HLIrs10777317
Exacrs10777317
Varsomers10777317
Maprs10777317
PheGenIrs10777317
hapmaprs10777317
1000 genomesrs10777317
hgdprs10777317
ensemblrs10777317
gopubmedrs10777317
geneviewrs10777317
scholarrs10777317
googlers10777317
pharmgkbrs10777317
gwascentralrs10777317
openSNPrs10777317
23andMers10777317
23andMe allrs10777317
SNP Nexus

SNPshotrs10777317
SNPdbers10777317
MSV3drs10777317
GWAS Ctlgrs10777317
GMAF0.4399
Max Magnitude
? (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 0.000005
Odds Ratio 1.1200 [1.07-1.18]