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rs9308762

From SNPedia

Orientationplus
Stabilizedplus
Make rs9308762(C;C)
Make rs9308762(C;T)
Make rs9308762(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position118106298
GeneINSIG2
is asnp
is mentioned by
dbSNPrs9308762
ebirs9308762
HLIrs9308762
Exacrs9308762
Varsomers9308762
Maprs9308762
PheGenIrs9308762
hapmaprs9308762
1000 genomesrs9308762
hgdprs9308762
ensemblrs9308762
gopubmedrs9308762
geneviewrs9308762
scholarrs9308762
googlers9308762
pharmgkbrs9308762
gwascentralrs9308762
openSNPrs9308762
23andMers9308762
23andMe allrs9308762
SNP Nexus

SNPshotrs9308762
SNPdbers9308762
MSV3drs9308762
GWAS Ctlgrs9308762
GMAF0.2755
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 19360016OA-icon.png] INSIG2 SNPs Associated With Obesity and Glucose Homeostasis Traits in Hispanics: The IRAS Family Study


[PMID 20028541OA-icon.png] A tagging SNP in INSIG2 is associated with obesity-related phenotypes among Samoans


[PMID 22968099OA-icon.png] INSIG2 variants, dietary patterns and metabolic risk in Samoa.