Variant (rsID / SNP)
rs397517408
rs397517408 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSC2. Location: chromosome 18, position 28,673,580. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
DSC2Pathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- Deletion
- Chromosome / position
- 18:28673580
- Cytoband
- 18q12.1
- HGVS
- NM_024422.6(DSC2):c.96del (p.Ala31_Cys32insTer)
Associated conditions / phenotypes
Arrhythmogenic right ventricular cardiomyopathy|Cardiomyopathy|Arrhythmogenic right ventricular dysplasia 11
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.