Gene entry
SCN10A
sodium voltage-gated channel alpha subunit 10
- Chromosome
- 3
- Cytoband
- 3p22.2
- Variants (rsID)
- 64
SCN10A is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3p22.2). Its official name is “sodium voltage-gated channel alpha subunit 10”. The reference table lists 64 variants (rsID) for this gene.
Clinically classified variants
24 reference-table entries with clinical significance.
- rs12632942Benignsingle nucleotide variantBrugada syndrome|Episodic pain syndrome, familial, 2
- rs144270136Benignsingle nucleotide variantBrugada syndrome
- rs150773437Benignsingle nucleotide variantBrugada syndrome
- rs151153639Benignsingle nucleotide variantBrugada syndrome
- rs4076737Benignsingle nucleotide variant
- rs57326399Benignsingle nucleotide variantBrugada syndrome|Episodic pain syndrome, familial, 2
- rs6599242Benignsingle nucleotide variantBrugada syndrome|Episodic pain syndrome, familial, 2
- rs6599250Benignsingle nucleotide variantBrugada syndrome|Episodic pain syndrome, familial, 2
- rs6795970Benignsingle nucleotide variantBrugada syndrome|Episodic pain syndrome, familial, 2
- rs6798015Benignsingle nucleotide variant
- rs73062575Benignsingle nucleotide variantBrugada syndrome
- rs7372672Benignsingle nucleotide variant
- rs7374804Benignsingle nucleotide variantBrugada syndrome
- rs7431144Benignsingle nucleotide variant
- rs7433306Benignsingle nucleotide variant
- rs7617919Benignsingle nucleotide variantBrugada syndrome|Episodic pain syndrome, familial, 2
- rs77804526Benignsingle nucleotide variantBrugada syndrome
- rs78555408Benignsingle nucleotide variantBrugada syndrome
- rs138404783Conflicting interpretationssingle nucleotide variantEpisodic pain syndrome, familial, 2|Brugada syndrome
- rs138832868Conflicting interpretationssingle nucleotide variantBrugada syndrome 1|Episodic pain syndrome, familial, 2|Brugada syndrome
- rs141207048Likely benignsingle nucleotide variantBrugada syndrome|Episodic pain syndrome, familial, 2|Brugada syndrome 1
- rs142217269Likely benignsingle nucleotide variantBrugada syndrome
- rs199973777Likely benignsingle nucleotide variantBrugada syndrome
- rs192493052Uncertain significancesingle nucleotide variantBrugada syndrome
Other listed variants
- rs4676595
- rs6599240
- rs6599254
- rs6783110
- rs6798701
- rs6800541
- rs6801957
- rs7429946
- rs7430477
- rs7611456
- rs7627881
- rs7635221
- rs7651106
- rs9815891
- rs9820042
- rs9825762
- rs10428132
- rs11129806
- rs11927856
- rs12636123
- rs59856101
- rs62244071
- rs73826323
- rs79267898
- rs118033509
- rs138738471
- rs139988577
- rs186031413
- rs189929388
- rs191056911
- rs191389107
- rs191397931
- rs191869263
- rs199703203
- rs199734710
- rs199892190
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.