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rs10185316

From SNPedia

Orientationplus
Stabilizedplus
Make rs10185316(C;C)
Make rs10185316(C;G)
Make rs10185316(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position118086902
GeneINSIG2
is asnp
is mentioned by
dbSNPrs10185316
ebirs10185316
HLIrs10185316
Exacrs10185316
Varsomers10185316
Maprs10185316
PheGenIrs10185316
hapmaprs10185316
1000 genomesrs10185316
hgdprs10185316
ensemblrs10185316
gopubmedrs10185316
geneviewrs10185316
scholarrs10185316
googlers10185316
pharmgkbrs10185316
gwascentralrs10185316
openSNPrs10185316
23andMers10185316
23andMe allrs10185316
SNP Nexus

SNPshotrs10185316
SNPdbers10185316
MSV3drs10185316
GWAS Ctlgrs10185316
GMAF0.2612
Max Magnitude
? (C;C) (C;G) (G;G) 28
[PMID 20045156OA-icon.png] Common INSIG2 polymorphisms are associated with age-related changes in body size and high-density lipoprotein cholesterol from young adulthood to middle age

[PMID 20877301] Gene-gene interactions of the INSIG1 and INSIG2 in metabolic syndrome in schizophrenic patients treated with atypical antipsychotics.