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rs286913

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs286913(C;T)
Make rs286913(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position34633816
GeneEHF
is asnp
is mentioned by
dbSNPrs286913
ebirs286913
HLIrs286913
Exacrs286913
Varsomers286913
Maprs286913
PheGenIrs286913
hapmaprs286913
1000 genomesrs286913
hgdprs286913
ensemblrs286913
gopubmedrs286913
geneviewrs286913
scholarrs286913
googlers286913
pharmgkbrs286913
gwascentralrs286913
openSNPrs286913
23andMers286913
23andMe allrs286913
SNP Nexus

SNPshotrs286913
SNPdbers286913
MSV3drs286913
GWAS Ctlgrs286913
GMAF0.06015
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 7E-8
Odds Ratio None None