rs7236632
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7236632(A;A) |
Make rs7236632(A;G) |
Make rs7236632(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 18 |
Position | 57766970 |
Gene | ATP8B1 |
is a | snp |
is | mentioned by |
dbSNP | rs7236632 |
dbSNP (classic) | rs7236632 |
ClinGen | rs7236632 |
ebi | rs7236632 |
HLI | rs7236632 |
Exac | rs7236632 |
Gnomad | rs7236632 |
Varsome | rs7236632 |
LitVar | rs7236632 |
Map | rs7236632 |
PheGenI | rs7236632 |
Biobank | rs7236632 |
1000 genomes | rs7236632 |
hgdp | rs7236632 |
ensembl | rs7236632 |
geneview | rs7236632 |
scholar | rs7236632 |
rs7236632 | |
pharmgkb | rs7236632 |
gwascentral | rs7236632 |
openSNP | rs7236632 |
23andMe | rs7236632 |
SNPshot | rs7236632 |
SNPdbe | rs7236632 |
MSV3d | rs7236632 |
GWAS Ctlg | rs7236632 |
GMAF | 0.2438 |
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 |