Variant (rsID / SNP)
rs869025522
rs869025522 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,597,210. Clinical significance in the table: Likely pathogenic.
Reference-table entries
SCN5ALikely pathogenic
- Clinical significance (as recorded)
- Likely pathogenic
- Variant type
- Microsatellite
- Chromosome / position
- 3:38597210
- Cytoband
- 3p22.2
- HGVS
- NM_000335.5(SCN5A):c.4471AAG[1] (p.Lys1492del)
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.