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rs10490625

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10490625(C;T)
Make rs10490625(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position118101980
GeneINSIG2
is asnp
is mentioned by
dbSNPrs10490625
ebirs10490625
HLIrs10490625
Exacrs10490625
Varsomers10490625
Maprs10490625
PheGenIrs10490625
hapmaprs10490625
1000 genomesrs10490625
hgdprs10490625
ensemblrs10490625
gopubmedrs10490625
geneviewrs10490625
scholarrs10490625
googlers10490625
pharmgkbrs10490625
gwascentralrs10490625
openSNPrs10490625
23andMers10490625
23andMe allrs10490625
SNP Nexus

SNPshotrs10490625
SNPdbers10490625
MSV3drs10490625
GWAS Ctlgrs10490625
GMAF0.05188
Max Magnitude0
? (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