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rs12726652

From SNPedia

Orientationplus
Stabilizedplus
Make rs12726652(A;A)
Make rs12726652(A;G)
Make rs12726652(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position106889954
is asnp
is mentioned by
dbSNPrs12726652
dbSNP (classic)rs12726652
ClinGenrs12726652
ebirs12726652
HLIrs12726652
Exacrs12726652
Gnomadrs12726652
Varsomers12726652
LitVarrs12726652
Maprs12726652
PheGenIrs12726652
Biobankrs12726652
1000 genomesrs12726652
hgdprs12726652
ensemblrs12726652
geneviewrs12726652
scholarrs12726652
googlers12726652
pharmgkbrs12726652
gwascentralrs12726652
openSNPrs12726652
23andMers12726652
SNPshotrs12726652
SNPdbers12726652
MSV3drs12726652
GWAS Ctlgrs12726652
GMAF0.2984
Max Magnitude0
? (A;A) (A;G) (G;G) 28


GWAS snp
PMID [PMID 21107309OA-icon.png]
Trait
Title Genome-Wide Pharmacogenomic Study of Neurocognition As an Indicator of Antipsychotic Treatment Response in Schizophrenia
Risk Allele
P-val 5E-7
Odds Ratio None None