rs9512900
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs9512900(C;C) |
Make rs9512900(C;T) |
Make rs9512900(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 13 |
Position | 27855601 |
Gene | PDX1-AS1 |
is a | snp |
is | mentioned by |
dbSNP | rs9512900 |
dbSNP (classic) | rs9512900 |
ClinGen | rs9512900 |
ebi | rs9512900 |
HLI | rs9512900 |
Exac | rs9512900 |
Gnomad | rs9512900 |
Varsome | rs9512900 |
LitVar | rs9512900 |
Map | rs9512900 |
PheGenI | rs9512900 |
Biobank | rs9512900 |
1000 genomes | rs9512900 |
hgdp | rs9512900 |
ensembl | rs9512900 |
geneview | rs9512900 |
scholar | rs9512900 |
rs9512900 | |
pharmgkb | rs9512900 |
gwascentral | rs9512900 |
openSNP | rs9512900 |
23andMe | rs9512900 |
SNPshot | rs9512900 |
SNPdbe | rs9512900 |
MSV3d | rs9512900 |
GWAS Ctlg | rs9512900 |
GMAF | 0.1653 |
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 | 0.000009 |
Odds Ratio | NR NR |