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rs11587682

From SNPedia

Orientationplus
Stabilizedplus
Make rs11587682(C;C)
Make rs11587682(C;T)
Make rs11587682(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position150351808
GenePRPF3
is asnp
is mentioned by
dbSNPrs11587682
dbSNP (classic)rs11587682
ClinGenrs11587682
ebirs11587682
HLIrs11587682
Exacrs11587682
Gnomadrs11587682
Varsomers11587682
LitVarrs11587682
Maprs11587682
PheGenIrs11587682
Biobankrs11587682
1000 genomesrs11587682
hgdprs11587682
ensemblrs11587682
geneviewrs11587682
scholarrs11587682
googlers11587682
pharmgkbrs11587682
gwascentralrs11587682
openSNPrs11587682
23andMers11587682
SNPshotrs11587682
SNPdbers11587682
MSV3drs11587682
GWAS Ctlgrs11587682
GMAF0.06336
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 23453885OA-icon.png]
Trait Autism spectrum disorder, attention deficit-hyperactivity disorder, bipolar disorder, major depressive disorder, and schizophrenia (combined)
Title Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.
Risk Allele C
P-val 7E-6
Odds Ratio 1.09 [1.05-1.12]