Variant (rsID / SNP)
rs41313681
rs41313681 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,640,465. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
SCN5ABenign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:38640465
- Cytoband
- 3p22.2
- HGVS
- NM_000335.5(SCN5A):c.1967C>T (p.Pro656Leu)
- Allele change
- Missense_P656L
Associated conditions / phenotypes
Brugada syndrome|Sick sinus syndrome 1|Long QT syndrome 3|Dilated cardiomyopathy 1E|Progressive familial heart block, type 1A|Brugada syndrome 1|Ventricular fibrillation, paroxysmal familial, type 1|Cardiac arrhythmia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.