rs10229603
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10229603(C;C) |
Make rs10229603(C;T) |
Make rs10229603(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 112988318 |
Gene | HRAT17 |
is a | snp |
is | mentioned by |
dbSNP | rs10229603 |
dbSNP (classic) | rs10229603 |
ClinGen | rs10229603 |
ebi | rs10229603 |
HLI | rs10229603 |
Exac | rs10229603 |
Gnomad | rs10229603 |
Varsome | rs10229603 |
LitVar | rs10229603 |
Map | rs10229603 |
PheGenI | rs10229603 |
Biobank | rs10229603 |
1000 genomes | rs10229603 |
hgdp | rs10229603 |
ensembl | rs10229603 |
geneview | rs10229603 |
scholar | rs10229603 |
rs10229603 | |
pharmgkb | rs10229603 |
gwascentral | rs10229603 |
openSNP | rs10229603 |
23andMe | rs10229603 |
SNPshot | rs10229603 |
SNPdbe | rs10229603 |
MSV3d | rs10229603 |
GWAS Ctlg | rs10229603 |
GMAF | 0.2567 |
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 |