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rs2159767

From SNPedia

Orientationplus
Stabilizedplus
Make rs2159767(C;C)
Make rs2159767(C;T)
Make rs2159767(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position148299501
is asnp
is mentioned by
dbSNPrs2159767
ebirs2159767
HLIrs2159767
Exacrs2159767
Varsomers2159767
Maprs2159767
PheGenIrs2159767
hapmaprs2159767
1000 genomesrs2159767
hgdprs2159767
ensemblrs2159767
gopubmedrs2159767
geneviewrs2159767
scholarrs2159767
googlers2159767
pharmgkbrs2159767
gwascentralrs2159767
openSNPrs2159767
23andMers2159767
23andMe allrs2159767
SNP Nexus

SNPshotrs2159767
SNPdbers2159767
MSV3drs2159767
GWAS Ctlgrs2159767
GMAF0.3761
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 18347602OA-icon.png]
Trait Schizophrenia
Title Genomewide association for schizophrenia in the CATIE study: results of stage 1
Risk Allele
P-val 0.0000069999999999999999
Odds Ratio 1.33 [NR]


GET Evidence
rs2159767
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.576087
summary