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Variant (rsID / SNP)

rs200868190

SCN5A

rs200868190 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,645,359. 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
3:38645359
Cytoband
3p22.2
HGVS
NM_000335.5(SCN5A):c.1734C>T (p.Pro578=)
Allele change
Synonymous_P578P

Associated conditions / phenotypes

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.