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Variant (rsID / SNP)

rs199473068

SCN5A

rs199473068 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,662,377. 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
3:38662377
Cytoband
3p22.2
HGVS
NM_000335.5(SCN5A):c.568C>G (p.Arg190Gly)
Allele change
Missense_R190G

Associated conditions / phenotypes

Congenital long QT syndrome|Cardiac arrhythmia|Brugada syndrome

Public references

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