rs8041675
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs8041675(C;C) |
| Make rs8041675(C;T) |
| Make rs8041675(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 37050401 |
| Gene | MEIS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs8041675 |
| dbSNP (classic) | rs8041675 |
| ClinGen | rs8041675 |
| ebi | rs8041675 |
| HLI | rs8041675 |
| Exac | rs8041675 |
| Gnomad | rs8041675 |
| Varsome | rs8041675 |
| LitVar | rs8041675 |
| Map | rs8041675 |
| PheGenI | rs8041675 |
| Biobank | rs8041675 |
| 1000 genomes | rs8041675 |
| hgdp | rs8041675 |
| ensembl | rs8041675 |
| geneview | rs8041675 |
| scholar | rs8041675 |
| rs8041675 | |
| pharmgkb | rs8041675 |
| gwascentral | rs8041675 |
| openSNP | rs8041675 |
| 23andMe | rs8041675 |
| SNPshot | rs8041675 |
| SNPdbe | rs8041675 |
| MSV3d | rs8041675 |
| GWAS Ctlg | rs8041675 |
| GMAF | 0.4467 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 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 | 0.000004 |
| Odds Ratio | NR NR |
