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| Official Symbol of Gene | SCN10A |
| Species | Homo sapiens |
| Entrez Gene ID | 6336 |
| Official Full Name | sodium voltage-gated channel alpha subunit 10 |
| Also known as | PN3; SNS; FEPS2; Nav1.8 |
| Gene Type | protein coding |
| dbXrefs | Ensembl:ENSG00000185313 MIM:604427; AllianceGenome:HGNC:10582 |
| Map Location | 3p22.2 |
| Variation Type | SNP |
| refSNP ID | rs6795970 |
| Detected Sample | N/A |
| Sample Detail | N/A |
| Detected Method | N/A |
| Disease | MS |
| Disease subtype | N/A |
| Population | N/A |
| Sample Size | 161 patients with relapsing-onset MS and 94 demographically comparable healthy participants |
| Pubmed ID | 26740675 |
| Year | 2016 |
| Title | Channelopathy-related SCN10A gene variants predict cerebellar dysfunction in multiple sclerosis |
| Risk Type | Phenotypic risk |
| Main Result | Positive |
| Result | Two SCN10A polymorphisms in high linkage disequilibrium showed significant association with MSFC performance in patients with MS. |
| Mechanism/Pathway | N/A |

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