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rs17126180

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs17126180(C;G)
Make rs17126180(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position51870172
is asnp
is mentioned by
dbSNPrs17126180
ebirs17126180
HLIrs17126180
Exacrs17126180
Varsomers17126180
Maprs17126180
PheGenIrs17126180
hapmaprs17126180
1000 genomesrs17126180
hgdprs17126180
ensemblrs17126180
gopubmedrs17126180
geneviewrs17126180
scholarrs17126180
googlers17126180
pharmgkbrs17126180
gwascentralrs17126180
openSNPrs17126180
23andMers17126180
23andMe allrs17126180
SNP Nexus

SNPshotrs17126180
SNPdbers17126180
MSV3drs17126180
GWAS Ctlgrs17126180
GMAF0.1125
Max Magnitude0
? (C;C) (C;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 9E-7
Odds Ratio None None