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rs4741652

From SNPedia

Orientationplus
Stabilizedplus
Make rs4741652(C;C)
Make rs4741652(C;T)
Make rs4741652(T;T)
ReferenceGRCh37.p5 37.3/137
Chromosome9
Position2194227
GeneLOC107987043
is asnp
is mentioned by
dbSNPrs4741652
dbSNP (classic)rs4741652
ClinGenrs4741652
ebirs4741652
HLIrs4741652
Exacrs4741652
Gnomadrs4741652
Varsomers4741652
LitVarrs4741652
Maprs4741652
PheGenIrs4741652
Biobankrs4741652
1000 genomesrs4741652
hgdprs4741652
ensemblrs4741652
geneviewrs4741652
scholarrs4741652
googlers4741652
pharmgkbrs4741652
gwascentralrs4741652
openSNPrs4741652
23andMers4741652
SNPshotrs4741652
SNPdbers4741652
MSV3drs4741652
GWAS Ctlgrs4741652
GMAF0.2291
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 T
P-val 7E-6
Odds Ratio 1.07 [1.04-1.12]