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Variant (rsID / SNP)

rs796756333

DSC2

rs796756333 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSC2. Location: chromosome 18, position 28,663,027. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

DSC2Conflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
18:28663027
Cytoband
18q12.1
HGVS
NM_024422.6(DSC2):c.943-1G>A
Allele change
Silent

Associated conditions / phenotypes

Arrhythmogenic right ventricular dysplasia 11|Cardiovascular phenotype|Cardiomyopathy

Public references

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