rs80356476
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs80356476(C;T) |
| Make rs80356476(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 166277252 |
| Gene | LOC101929680, SCN9A |
| is a | snp |
| is | mentioned by |
| dbSNP | rs80356476 |
| dbSNP (classic) | rs80356476 |
| ClinGen | rs80356476 |
| ebi | rs80356476 |
| HLI | rs80356476 |
| Exac | rs80356476 |
| Gnomad | rs80356476 |
| Varsome | rs80356476 |
| LitVar | rs80356476 |
| Map | rs80356476 |
| PheGenI | rs80356476 |
| Biobank | rs80356476 |
| 1000 genomes | rs80356476 |
| hgdp | rs80356476 |
| ensembl | rs80356476 |
| geneview | rs80356476 |
| scholar | rs80356476 |
| rs80356476 | |
| pharmgkb | rs80356476 |
| gwascentral | rs80356476 |
| openSNP | rs80356476 |
| 23andMe | rs80356476 |
| SNPshot | rs80356476 |
| SNPdbe | rs80356476 |
| MSV3d | rs80356476 |
| GWAS Ctlg | rs80356476 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs80356476(T;T) |
| Alt | rs80356476(T;T) |
| Reference | Rs80356476(C;C) |
| Significance | Pathogenic |
| Disease | Primary erythromelalgia |
| Variation | info |
| Gene | LOC101929680 SCN9A |
| CLNDBN | Primary erythromelalgia |
| Reversed | 1 |
| HGVS | NC_000002.11:g.167133762G>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000006736.3, |
[PMID 15955112] SCN9A mutations define primary erythermalgia as a neuropathic disorder of voltage gated sodium channels.
[PMID 16392115] Sporadic onset of erythermalgia: a gain-of-function mutation in Nav1.7.
