rs10250997
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10250997(A;A) |
Make rs10250997(A;C) |
Make rs10250997(C;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 136461788 |
is a | snp |
is | mentioned by |
dbSNP | rs10250997 |
dbSNP (classic) | rs10250997 |
ClinGen | rs10250997 |
ebi | rs10250997 |
HLI | rs10250997 |
Exac | rs10250997 |
Gnomad | rs10250997 |
Varsome | rs10250997 |
LitVar | rs10250997 |
Map | rs10250997 |
PheGenI | rs10250997 |
Biobank | rs10250997 |
1000 genomes | rs10250997 |
hgdp | rs10250997 |
ensembl | rs10250997 |
geneview | rs10250997 |
scholar | rs10250997 |
rs10250997 | |
pharmgkb | rs10250997 |
gwascentral | rs10250997 |
openSNP | rs10250997 |
23andMe | rs10250997 |
SNPshot | rs10250997 |
SNPdbe | rs10250997 |
MSV3d | rs10250997 |
GWAS Ctlg | rs10250997 |
GMAF | 0.09871 |
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 | C |
P-val | 8E-6 |
Odds Ratio | 1.03 [0.99-1.07] |