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Variant (rsID / SNP)

rs45563942

SCN5A

rs45563942 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SCN5A. Location: chromosome 3, position 38,592,356. 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
3:38592356
Cytoband
3p22.2
HGVS
NM_000335.5(SCN5A):c.5504T>C (p.Ile1835Thr)
Allele change
Missense_I1782T

Associated conditions / phenotypes

Dilated cardiomyopathy 1E|Primary dilated cardiomyopathy|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.