Variant (rsID / SNP)
rs794728888
rs794728888 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,592,993. 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
- 3:38592993
- Cytoband
- 3p22.2
- HGVS
- NM_000335.5(SCN5A):c.4867G>A (p.Val1623Ile)
- Allele change
- Missense_V1570I
Associated conditions / phenotypes
Long QT syndrome 3|Dilated cardiomyopathy 1E|Progressive familial heart block, type 1A|Ventricular fibrillation, paroxysmal familial, type 1|Sick sinus syndrome 1|Brugada syndrome 1|Brugada syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.