Variant (rsID / SNP)
rs886039018
rs886039018 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,597,946. Clinical significance in the table: Pathogenic.
Reference-table entries
SCN5APathogenic
- Clinical significance (as recorded)
- Pathogenic
- Variant type
- Deletion
- Chromosome / position
- 3:38597946
- Cytoband
- 3p22.2
- HGVS
- NM_000335.5(SCN5A):c.4420del (p.Gln1474fs)
Associated conditions / phenotypes
Cardiovascular phenotype
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.