Variant (rsID / SNP)
rs67701503
rs67701503 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN1B. Location: chromosome 19, position 35,524,939. Clinical significance in the table: Benign.
Reference-table entries
SCN1BBenign
- Clinical significance (as recorded)
- Benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 19:35524939
- Cytoband
- 19q13.11
- HGVS
- NM_001037.5(SCN1B):c.448+296C>A
- Allele change
- Missense_S248R
Associated conditions / phenotypes
Brugada syndrome 5
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.