Variant (rsID / SNP)
rs199473606
rs199473606 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,601,848. The table records no clinical significance for this variant.
Reference-table entries
SCN5ANot classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:38601848
- Cytoband
- 3p22.2
- HGVS
- NM_000335.5(SCN5A):c.4032G>T (p.Trp1344Cys)
- Allele change
- Nonsense_W1291X
Associated conditions / phenotypes
Brugada syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.