Variant (rsID / SNP)

rs794728149

rs794728149 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSP. Location: chromosome 6, position 7,585,367. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DSPPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: Duplication
Chromosome / position: 6:7585367
Cytoband: 6p24.3
HGVS: NM_004415.4(DSP):c.7873dup (p.Thr2625fs)

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.