rs478597
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs478597(C;C) |
| Make rs478597(C;T) |
| Make rs478597(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 117313620 |
| Gene | NOS1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs478597 |
| dbSNP (classic) | rs478597 |
| ClinGen | rs478597 |
| ebi | rs478597 |
| HLI | rs478597 |
| Exac | rs478597 |
| Gnomad | rs478597 |
| Varsome | rs478597 |
| LitVar | rs478597 |
| Map | rs478597 |
| PheGenI | rs478597 |
| Biobank | rs478597 |
| 1000 genomes | rs478597 |
| hgdp | rs478597 |
| ensembl | rs478597 |
| geneview | rs478597 |
| scholar | rs478597 |
| rs478597 | |
| pharmgkb | rs478597 |
| gwascentral | rs478597 |
| openSNP | rs478597 |
| 23andMe | rs478597 |
| SNPshot | rs478597 |
| SNPdbe | rs478597 |
| MSV3d | rs478597 |
| GWAS Ctlg | rs478597 |
| GMAF | 0.3104 |
| 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 | 0.000008 |
| Odds Ratio | NR NR |
[PMID 18663495
] Nitric oxide synthase genes and their interactions with environmental factors in Parkinson's disease.
