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rs9315632

From SNPedia

Orientationplus
Stabilizedplus
Make rs9315632(G;G)
Make rs9315632(G;T)
Make rs9315632(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position38942490
is asnp
is mentioned by
dbSNPrs9315632
ebirs9315632
HLIrs9315632
Exacrs9315632
Varsomers9315632
Maprs9315632
PheGenIrs9315632
hapmaprs9315632
1000 genomesrs9315632
hgdprs9315632
ensemblrs9315632
gopubmedrs9315632
geneviewrs9315632
scholarrs9315632
googlers9315632
pharmgkbrs9315632
gwascentralrs9315632
openSNPrs9315632
23andMers9315632
23andMe allrs9315632
SNP Nexus

SNPshotrs9315632
SNPdbers9315632
MSV3drs9315632
GWAS Ctlgrs9315632
GMAF0.2645
Max Magnitude
? (G;G) (G;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 0.000003
Odds Ratio None None