rs10815798
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10815798(A;A) |
Make rs10815798(A;G) |
Make rs10815798(G;G) |
Reference | GRCh37 37.1/131 |
Chromosome | 9 |
Position | 8235633 |
is a | snp |
is | mentioned by |
dbSNP | rs10815798 |
dbSNP (classic) | rs10815798 |
ClinGen | rs10815798 |
ebi | rs10815798 |
HLI | rs10815798 |
Exac | rs10815798 |
Gnomad | rs10815798 |
Varsome | rs10815798 |
LitVar | rs10815798 |
Map | rs10815798 |
PheGenI | rs10815798 |
Biobank | rs10815798 |
1000 genomes | rs10815798 |
hgdp | rs10815798 |
ensembl | rs10815798 |
geneview | rs10815798 |
scholar | rs10815798 |
rs10815798 | |
pharmgkb | rs10815798 |
gwascentral | rs10815798 |
openSNP | rs10815798 |
23andMe | rs10815798 |
SNPshot | rs10815798 |
SNPdbe | rs10815798 |
MSV3d | rs10815798 |
GWAS Ctlg | rs10815798 |
GMAF | 0.4435 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 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 | A |
P-val | 0.000006 |
Odds Ratio | NR NR |