Variant (rsID / SNP)
rs41313693
rs41313693 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,645,524. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
SCN5AConflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:38645524
- Cytoband
- 3p22.2
- HGVS
- NM_000335.5(SCN5A):c.1569T>A (p.Arg523=)
- Allele change
- Synonymous_R523R
Associated conditions / phenotypes
Brugada syndrome|Long QT syndrome|Congenital long QT syndrome|Sick sinus syndrome|Paroxysmal familial ventricular fibrillation|Progressive familial heart block|Dilated Cardiomyopathy, Dominant|Cardiovascular phenotype|Cardiac arrhythmia
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.