Variant (rsID / SNP)

rs794728136

rs794728136 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSP. Location: chromosome 6, position 7,556,053. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

DSPPathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: Deletion
Chromosome / position: 6:7556053
Cytoband: 6p24.3
HGVS: NM_004415.4(DSP):c.273del (p.Glu92fs)

Associated conditions / phenotypes

Primary dilated cardiomyopathy|Arrhythmogenic right ventricular cardiomyopathy

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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