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rs3813928

From SNPedia

Orientationplus
Stabilizedplus
Make rs3813928(A;A)
Make rs3813928(A;G)
Make rs3813928(G;G)
ReferenceGRCh38 38.1/141
ChromosomeX
Position114583809
GeneHTR2C
is asnp
is mentioned by
dbSNPrs3813928
ebirs3813928
HLIrs3813928
Exacrs3813928
Varsomers3813928
Maprs3813928
PheGenIrs3813928
hapmaprs3813928
1000 genomesrs3813928
hgdprs3813928
ensemblrs3813928
gopubmedrs3813928
geneviewrs3813928
scholarrs3813928
googlers3813928
pharmgkbrs3813928
gwascentralrs3813928
openSNPrs3813928
23andMers3813928
23andMe allrs3813928
SNP Nexus

SNPshotrs3813928
SNPdbers3813928
MSV3drs3813928
GWAS Ctlgrs3813928
GMAF0.1167
Max Magnitude
? (A;A) (A;G) (G;G) 28
rs3813928 (-995G>A / G-995A) is a SNP upstream of HTR2C.

[PMID 19997080] in a small sample of 45 autistic patients taking risperidone for up to one year, HTR2A Rs6311 (-1438G>A), DRD3 rs6280 (Ser9Gly), HTR2C rs3813928 (995G>A) and ABCB1 rs1128503) (1236C>T) were predictive of risperidone response


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


[PMID 15717931OA-icon.png] Identification of functional SNPs in the 5-prime flanking sequences of human genes.

[PMID 17016522] The association between HTR2C polymorphisms and obesity in psychiatric patients using antipsychotics: a cross-sectional study.

[PMID 17632216] The association between HTR2C gene polymorphisms and the metabolic syndrome in patients with schizophrenia.


GET Evidence
rs3813928
aa_change
aa_change_short
impact pharmacogenetic
qualified_impact Insufficiently evaluated pharmacogenetic
overall_frequency 0.0978261
summary