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Variant (rsID / SNP)

rs34884895

DSP

rs34884895 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSP. Location: chromosome 6, position 7,585,795. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

DSPBenign
Clinical significance (as recorded)
Benign/Likely benign
Variant type
single nucleotide variant
Chromosome / position
6:7585795
Cytoband
6p24.3
HGVS
NM_004415.4(DSP):c.8300C>A (p.Thr2767Asn)
Allele change
Missense_T2324N

Associated conditions / phenotypes

Arrhythmogenic cardiomyopathy with woolly hair and keratoderma|Arrhythmogenic right ventricular dysplasia 8|Epidermolysis bullosa simplex due to plakophilin deficiency|Lethal acantholytic epidermolysis bullosa|Arrhythmogenic right ventricular cardiomyopathy|Skin fragility-woolly hair-palmoplantar keratoderma syndrome|Cardiomyopathy|Hypertrophic cardiomyopathy|Systolic heart failure

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.