rs910191
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs910191(C;C) |
| Make rs910191(C;T) |
| Make rs910191(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 20 |
| Position | 48460486 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs910191 |
| dbSNP (classic) | rs910191 |
| ClinGen | rs910191 |
| ebi | rs910191 |
| HLI | rs910191 |
| Exac | rs910191 |
| Gnomad | rs910191 |
| Varsome | rs910191 |
| LitVar | rs910191 |
| Map | rs910191 |
| PheGenI | rs910191 |
| Biobank | rs910191 |
| 1000 genomes | rs910191 |
| hgdp | rs910191 |
| ensembl | rs910191 |
| geneview | rs910191 |
| scholar | rs910191 |
| rs910191 | |
| pharmgkb | rs910191 |
| gwascentral | rs910191 |
| openSNP | rs910191 |
| 23andMe | rs910191 |
| SNPshot | rs910191 |
| SNPdbe | rs910191 |
| MSV3d | rs910191 |
| GWAS Ctlg | rs910191 |
| GMAF | 0.4004 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 23527680] |
| Trait | Attention deficit hyperactivity disorder (combined symptoms) |
| Title | Genome-wide association study of inattention and hyperactivity-impulsivity measured as quantitative traits. |
| Risk Allele | A |
| P-val | 2E-6 |
| Odds Ratio | NR NR |
