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rs16865258

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs16865258(C;T)
Make rs16865258(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position190279607
is asnp
is mentioned by
dbSNPrs16865258
ebirs16865258
HLIrs16865258
Exacrs16865258
Varsomers16865258
Maprs16865258
PheGenIrs16865258
hapmaprs16865258
1000 genomesrs16865258
hgdprs16865258
ensemblrs16865258
gopubmedrs16865258
geneviewrs16865258
scholarrs16865258
googlers16865258
pharmgkbrs16865258
gwascentralrs16865258
openSNPrs16865258
23andMers16865258
23andMe allrs16865258
SNP Nexus

SNPshotrs16865258
SNPdbers16865258
MSV3drs16865258
GWAS Ctlgrs16865258
GMAF0.01928
Max Magnitude0
? (C;C) (C;T) (T;T) 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 0.000002
Odds Ratio None None