Variant (rsID / SNP)

rs1184921987

rs1184921987 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSP. Location: chromosome 6, position 7,571,761. Clinical significance in the table: Pathogenic.

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Reference-table entries

DSPPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 6:7571761
Cytoband: 6p24.3
HGVS: NM_004415.4(DSP):c.1847A>C (p.Gln616Pro)
Allele change: Missense_Q616P

Associated conditions / phenotypes

Cardiomyopathy, dilated, with woolly hair, keratoderma, and tooth agenesis

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.