rs11152369
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs11152369(A;A) |
Make rs11152369(A;C) |
Make rs11152369(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 55399097 |
Gene | TCF4 |
is a | snp |
is | mentioned by |
dbSNP | rs11152369 |
dbSNP (classic) | rs11152369 |
ClinGen | rs11152369 |
ebi | rs11152369 |
HLI | rs11152369 |
Exac | rs11152369 |
Gnomad | rs11152369 |
Varsome | rs11152369 |
LitVar | rs11152369 |
Map | rs11152369 |
PheGenI | rs11152369 |
Biobank | rs11152369 |
1000 genomes | rs11152369 |
hgdp | rs11152369 |
ensembl | rs11152369 |
geneview | rs11152369 |
scholar | rs11152369 |
rs11152369 | |
pharmgkb | rs11152369 |
gwascentral | rs11152369 |
openSNP | rs11152369 |
23andMe | rs11152369 |
SNPshot | rs11152369 |
SNPdbe | rs11152369 |
MSV3d | rs11152369 |
GWAS Ctlg | rs11152369 |
GMAF | 0.05096 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 23453885] |
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] |