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rs11152369

From SNPedia

Orientationplus
Stabilizedplus
Make rs11152369(A;A)
Make rs11152369(A;C)
Make rs11152369(C;C)
ReferenceGRCh38 38.1/141
Chromosome18
Position55399097
GeneTCF4
is asnp
is mentioned by
dbSNPrs11152369
ebirs11152369
HLIrs11152369
Exacrs11152369
Varsomers11152369
Maprs11152369
PheGenIrs11152369
hapmaprs11152369
1000 genomesrs11152369
hgdprs11152369
ensemblrs11152369
gopubmedrs11152369
geneviewrs11152369
scholarrs11152369
googlers11152369
pharmgkbrs11152369
gwascentralrs11152369
openSNPrs11152369
23andMers11152369
23andMe allrs11152369
SNP Nexus

SNPshotrs11152369
SNPdbers11152369
MSV3drs11152369
GWAS Ctlgrs11152369
GMAF0.05096
Max Magnitude
? (A;A) (A;C) (C;C) 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 A
P-val 2E-7
Odds Ratio 1.19 [1.12-1.28]