Variant (rsID / SNP)

rs397516929

rs397516929 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSP. Location: chromosome 6, position 7,578,093. 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: 6:7578093
Cytoband: 6p24.3
HGVS: NM_004415.4(DSP):c.2959T>C (p.Ser987Pro)
Allele change: Missense_S987P

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.