Basic information of SCN10A :

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	rs6801957

Sample information of multiple sclerosis:

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

Literature information of multiple sclerosis :

Pubmed ID	26740675
Year	2016
Title	Channelopathy-related SCN10A gene variants predict cerebellar dysfunction in multiple sclerosis

Results of 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