rs931812
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs931812(C;C) |
Make rs931812(C;T) |
Make rs931812(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 8 |
Position | 100907093 |
is a | snp |
is | mentioned by |
dbSNP | rs931812 |
dbSNP (classic) | rs931812 |
ClinGen | rs931812 |
ebi | rs931812 |
HLI | rs931812 |
Exac | rs931812 |
Gnomad | rs931812 |
Varsome | rs931812 |
LitVar | rs931812 |
Map | rs931812 |
PheGenI | rs931812 |
Biobank | rs931812 |
1000 genomes | rs931812 |
hgdp | rs931812 |
ensembl | rs931812 |
geneview | rs931812 |
scholar | rs931812 |
rs931812 | |
pharmgkb | rs931812 |
gwascentral | rs931812 |
openSNP | rs931812 |
23andMe | rs931812 |
SNPshot | rs931812 |
SNPdbe | rs931812 |
MSV3d | rs931812 |
GWAS Ctlg | rs931812 |
GMAF | 0.2314 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
GWAS snp | |
---|---|
PMID | [PMID 18951430] |
Trait | Attention-deficit/hyperactivity disorder and conduct disorder |
Title | Conduct disorder and ADHD: Evaluation of conduct problems as a categorical and quantitative trait in the international multicentre ADHD genetics study |
Risk Allele | C |
P-val | 0.000005 |
Odds Ratio | NR NR |