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Variant (rsID / SNP)

rs754221948

SCN5A

rs754221948 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,595,864. 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
3:38595864
Cytoband
3p22.2
HGVS
NM_000335.5(SCN5A):c.4716C>T (p.Gly1572=)
Allele change
Synonymous_G1519G

Associated conditions / phenotypes

Cardiovascular phenotype|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.