Variant (rsID / SNP)

rs397514045

rs397514045 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSP. Location: chromosome 6, position 7,585,273. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DSPPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Deletion
Chromosome / position: 6:7585273
Cytoband: 6p24.3
HGVS: NM_004415.4(DSP):c.7780del (p.Ser2594fs)

Associated conditions / phenotypes

Arrhythmogenic cardiomyopathy with woolly hair and keratoderma

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.