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Variant (rsID / SNP)

rs199473635

SCN5A

rs199473635 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,592,387. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

SCN5AConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
3:38592387
Cytoband
3p22.2
HGVS
NM_000335.5(SCN5A):c.5473C>T (p.Arg1825Cys)
Allele change
Missense_R1772C

Associated conditions / phenotypes

Atrial fibrillation|Brugada syndrome|Cardiac arrhythmia

Public references

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