rs7495052
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7495052(C;C) |
| Make rs7495052(C;T) |
| Make rs7495052(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 15 |
| Position | 92008799 |
| Gene | SLCO3A1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7495052 |
| dbSNP (classic) | rs7495052 |
| ClinGen | rs7495052 |
| ebi | rs7495052 |
| HLI | rs7495052 |
| Exac | rs7495052 |
| Gnomad | rs7495052 |
| Varsome | rs7495052 |
| LitVar | rs7495052 |
| Map | rs7495052 |
| PheGenI | rs7495052 |
| Biobank | rs7495052 |
| 1000 genomes | rs7495052 |
| hgdp | rs7495052 |
| ensembl | rs7495052 |
| geneview | rs7495052 |
| scholar | rs7495052 |
| rs7495052 | |
| pharmgkb | rs7495052 |
| gwascentral | rs7495052 |
| openSNP | rs7495052 |
| 23andMe | rs7495052 |
| SNPshot | rs7495052 |
| SNPdbe | rs7495052 |
| MSV3d | rs7495052 |
| GWAS Ctlg | rs7495052 |
| GMAF | 0.477 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 18821565] |
| Trait | Inattentive 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 | 0.000003 |
| Odds Ratio | NR NR |
[PMID 20148275
] Shared heritability of attention-deficit/hyperactivity disorder and autism spectrum disorder.
