rs1415259
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Make rs1415259(A;A) |
| Make rs1415259(A;G) |
| Make rs1415259(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 1 |
| Position | 162115519 |
| Gene | LOC105371475, NOS1AP |
| is a | snp |
| is | mentioned by |
| dbSNP | rs1415259 |
| dbSNP (classic) | rs1415259 |
| ClinGen | rs1415259 |
| ebi | rs1415259 |
| HLI | rs1415259 |
| Exac | rs1415259 |
| Gnomad | rs1415259 |
| Varsome | rs1415259 |
| LitVar | rs1415259 |
| Map | rs1415259 |
| PheGenI | rs1415259 |
| Biobank | rs1415259 |
| 1000 genomes | rs1415259 |
| hgdp | rs1415259 |
| ensembl | rs1415259 |
| geneview | rs1415259 |
| scholar | rs1415259 |
| rs1415259 | |
| pharmgkb | rs1415259 |
| gwascentral | rs1415259 |
| openSNP | rs1415259 |
| 23andMe | rs1415259 |
| SNPshot | rs1415259 |
| SNPdbe | rs1415259 |
| MSV3d | rs1415259 |
| GWAS Ctlg | rs1415259 |
| GMAF | 0.4775 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
| GWAS snp | |
|---|---|
| PMID | [PMID 20062061] |
| Trait | Electrocardiographic traits |
| Title | Genetic variation in SCN10A influences cardiac conduction |
| Risk Allele | A |
| P-val | 7E-10 |
| Odds Ratio | 2.53 [1.73-3.33] ms decrease |
[PMID 20031603
] A genome-wide association scan of RR and QT interval duration in 3 European genetically isolated populations: the EUROSPAN project.
