rs17641078
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs17641078(C;C) |
| Make rs17641078(C;G) |
| Make rs17641078(G;G) |
| Reference | GRCh37 37.1/131 |
| Chromosome | 9 |
| Position | 1056959 |
| Gene | DMRT2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17641078 |
| dbSNP (classic) | rs17641078 |
| ClinGen | rs17641078 |
| ebi | rs17641078 |
| HLI | rs17641078 |
| Exac | rs17641078 |
| Gnomad | rs17641078 |
| Varsome | rs17641078 |
| LitVar | rs17641078 |
| Map | rs17641078 |
| PheGenI | rs17641078 |
| Biobank | rs17641078 |
| 1000 genomes | rs17641078 |
| hgdp | rs17641078 |
| ensembl | rs17641078 |
| geneview | rs17641078 |
| scholar | rs17641078 |
| rs17641078 | |
| pharmgkb | rs17641078 |
| gwascentral | rs17641078 |
| openSNP | rs17641078 |
| 23andMe | rs17641078 |
| SNPshot | rs17641078 |
| SNPdbe | rs17641078 |
| MSV3d | rs17641078 |
| GWAS Ctlg | rs17641078 |
| GMAF | 0.1175 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18821565] |
| Trait | Hyperactive-impulsive symptoms |
| Title | Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations |
| Risk Allele | |
| P-val | 0.000005 |
| Odds Ratio | NR NR |
