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Variant (rsID / SNP)

rs747448946

DSP

rs747448946 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSP. Location: chromosome 6, position 7,562,881. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

DSPConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
6:7562881
Cytoband
6p24.3
HGVS
NM_004415.4(DSP):c.598-4G>A
Allele change
Silent

Associated conditions / phenotypes

Primary familial hypertrophic cardiomyopathy|Arrhythmogenic cardiomyopathy with woolly hair and keratoderma|Arrhythmogenic right ventricular dysplasia 8|Cardiovascular phenotype|Cardiomyopathy

Public references

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