Variant (rsID / SNP)
rs199473156
rs199473156 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,629,036. The table records no clinical significance for this variant.
Reference-table entries
SCN5ANot classified
- Variant type
- single nucleotide variant
- Chromosome / position
- 3:38629036
- Cytoband
- 3p22.2
- HGVS
- NM_000335.5(SCN5A):c.2291T>G (p.Met764Arg)
- Allele change
- Missense_M764T
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.