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rs6764363

From SNPedia

Orientationplus
Stabilizedplus
Make rs6764363(C;C)
Make rs6764363(C;T)
Make rs6764363(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position270666
GeneCHL1
is asnp
is mentioned by
dbSNPrs6764363
ebirs6764363
HLIrs6764363
Exacrs6764363
Varsomers6764363
Maprs6764363
PheGenIrs6764363
hapmaprs6764363
1000 genomesrs6764363
hgdprs6764363
ensemblrs6764363
gopubmedrs6764363
geneviewrs6764363
scholarrs6764363
googlers6764363
pharmgkbrs6764363
gwascentralrs6764363
openSNPrs6764363
23andMers6764363
23andMe allrs6764363
SNP Nexus

SNPshotrs6764363
SNPdbers6764363
MSV3drs6764363
GWAS Ctlgrs6764363
GMAF0.2851
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 0.000006
Odds Ratio 1.1900 [1.10-1.28]