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rs10490624

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs10490624(A;G)
Make rs10490624(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position118104916
GeneINSIG2
is asnp
is mentioned by
dbSNPrs10490624
ebirs10490624
HLIrs10490624
Exacrs10490624
Varsomers10490624
Maprs10490624
PheGenIrs10490624
hapmaprs10490624
1000 genomesrs10490624
hgdprs10490624
ensemblrs10490624
gopubmedrs10490624
geneviewrs10490624
scholarrs10490624
googlers10490624
pharmgkbrs10490624
gwascentralrs10490624
openSNPrs10490624
23andMers10490624
23andMe allrs10490624
SNP Nexus

SNPshotrs10490624
SNPdbers10490624
MSV3drs10490624
GWAS Ctlgrs10490624
GMAF0.08953
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 20373477] Association study of polymorphisms in Insulin Induced Gene 2 (INSIG2) with antipsychotic-induced weight gain in European and African-American schizophrenia patients


[PMID 20504252] Association of HTR2C, but not LEP or INSIG2, genes with antipsychotic-induced weight gain in a German sample


[PMID 18195716] Association between the insulin-induced gene 2 (INSIG2) and weight gain in a German sample of antipsychotic-treated schizophrenic patients: perturbation of SREBP-controlled lipogenesis in drug-related metabolic adverse effects?