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rs489332

From SNPedia

Orientationplus
Stabilizedplus
Make rs489332(C;C)
Make rs489332(C;T)
Make rs489332(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position75413430
is asnp
is mentioned by
dbSNPrs489332
ebirs489332
HLIrs489332
Exacrs489332
Varsomers489332
Maprs489332
PheGenIrs489332
hapmaprs489332
1000 genomesrs489332
hgdprs489332
ensemblrs489332
gopubmedrs489332
geneviewrs489332
scholarrs489332
googlers489332
pharmgkbrs489332
gwascentralrs489332
openSNPrs489332
23andMers489332
23andMe allrs489332
SNP Nexus

SNPshotrs489332
SNPdbers489332
MSV3drs489332
GWAS Ctlgrs489332
GMAF0.1758
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23212062OA-icon.png]
Trait Schizophrenia
Title Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms.
Risk Allele
P-val 6E-6
Odds Ratio .11 [NR] unit decrease