Variant (rsID / SNP)

rs397514447

rs397514447 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,603,904. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SCN5APathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 3:38603904
Cytoband: 3p22.2
HGVS: NM_000335.5(SCN5A):c.3960+2T>C
Allele change: Silent

Associated conditions / phenotypes

Progressive familial heart block, type 1A|Brugada syndrome

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.