rs6765687
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6765687(C;C) |
Make rs6765687(C;T) |
Make rs6765687(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 52699090 |
Gene | GLT8D1 |
is a | snp |
is | mentioned by |
dbSNP | rs6765687 |
dbSNP (classic) | rs6765687 |
ClinGen | rs6765687 |
ebi | rs6765687 |
HLI | rs6765687 |
Exac | rs6765687 |
Gnomad | rs6765687 |
Varsome | rs6765687 |
LitVar | rs6765687 |
Map | rs6765687 |
PheGenI | rs6765687 |
Biobank | rs6765687 |
1000 genomes | rs6765687 |
hgdp | rs6765687 |
ensembl | rs6765687 |
geneview | rs6765687 |
scholar | rs6765687 |
rs6765687 | |
pharmgkb | rs6765687 |
gwascentral | rs6765687 |
openSNP | rs6765687 |
23andMe | rs6765687 |
SNPshot | rs6765687 |
SNPdbe | rs6765687 |
MSV3d | rs6765687 |
GWAS Ctlg | rs6765687 |
GMAF | 0.1928 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 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 | T |
P-val | 5E-6 |
Odds Ratio | 1.07 [1.04-1.11] |