Variant (rsID / SNP)

rs397516933

rs397516933 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSP. Location: chromosome 6, position 7,580,252. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

DSPLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 6:7580252
Cytoband: 6p24.3
HGVS: NM_004415.4(DSP):c.3829C>T (p.Gln1277Ter)
Allele change: Nonsense_Q1277X

Associated conditions / phenotypes

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.