Variant (rsID / SNP)

rs1064793890

rs1064793890 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSP. Location: chromosome 6, position 7,585,509. 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: 6:7585509
Cytoband: 6p24.3
HGVS: NM_004415.4(DSP):c.8014C>T (p.Gln2672Ter)
Allele change: Nonsense_Q2229X

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.