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rs17047764

From SNPedia

Orientationplus
Stabilizedplus
Make rs17047764(C;C)
Make rs17047764(C;G)
Make rs17047764(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position118111006
GeneINSIG2
is asnp
is mentioned by
dbSNPrs17047764
ebirs17047764
HLIrs17047764
Exacrs17047764
Varsomers17047764
Maprs17047764
PheGenIrs17047764
hapmaprs17047764
1000 genomesrs17047764
hgdprs17047764
ensemblrs17047764
gopubmedrs17047764
geneviewrs17047764
scholarrs17047764
googlers17047764
pharmgkbrs17047764
gwascentralrs17047764
openSNPrs17047764
23andMers17047764
23andMe allrs17047764
SNP Nexus

SNPshotrs17047764
SNPdbers17047764
MSV3drs17047764
GWAS Ctlgrs17047764
GMAF0.1905
Max Magnitude
? (C;C) (C;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?