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rs12957347

From SNPedia

Orientationplus
Stabilizedplus
Make rs12957347(C;C)
Make rs12957347(C;T)
Make rs12957347(T;T)
ReferenceGRCh38 38.1/141
Chromosome18
Position60083782
is asnp
is mentioned by
dbSNPrs12957347
ebirs12957347
HLIrs12957347
Exacrs12957347
Varsomers12957347
Maprs12957347
PheGenIrs12957347
hapmaprs12957347
1000 genomesrs12957347
hgdprs12957347
ensemblrs12957347
gopubmedrs12957347
geneviewrs12957347
scholarrs12957347
googlers12957347
pharmgkbrs12957347
gwascentralrs12957347
openSNPrs12957347
23andMers12957347
23andMe allrs12957347
SNP Nexus

SNPshotrs12957347
SNPdbers12957347
MSV3drs12957347
GWAS Ctlgrs12957347
GMAF0.2759
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20694148OA-icon.png]
Trait
Title A genome-wide association study of the metabolic syndrome in Indian Asian men
Risk Allele
P-val 0.000007
Odds Ratio None None