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rs2323266

From SNPedia

Orientationplus
Stabilizedplus
Make rs2323266(G;G)
Make rs2323266(G;T)
Make rs2323266(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position61391170
is asnp
is mentioned by
dbSNPrs2323266
dbSNP (classic)rs2323266
ClinGenrs2323266
ebirs2323266
HLIrs2323266
Exacrs2323266
Gnomadrs2323266
Varsomers2323266
LitVarrs2323266
Maprs2323266
PheGenIrs2323266
Biobankrs2323266
1000 genomesrs2323266
hgdprs2323266
ensemblrs2323266
geneviewrs2323266
scholarrs2323266
googlers2323266
pharmgkbrs2323266
gwascentralrs2323266
openSNPrs2323266
23andMers2323266
SNPshotrs2323266
SNPdbers2323266
MSV3drs2323266
GWAS Ctlgrs2323266
GMAF0.1451
Max Magnitude0
? (G;G) (G;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 3E-6
Odds Ratio .10 [NR] unit decrease