Variant (rsID / SNP)

rs869025399

rs869025399 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSP. Location: chromosome 6, position 7,583,219. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

DSPLikely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: Deletion
Chromosome / position: 6:7583219
Cytoband: 6p24.3
HGVS: NM_004415.4(DSP):c.5725del (p.Ile1909fs)

Associated conditions / phenotypes

Primary dilated 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.