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Variant (rsID / SNP)

rs62636492

DES

rs62636492 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DES. Location: chromosome 2, position 220,286,086. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

DESConflicting interpretations
Clinical significance (as recorded)
Conflicting interpretations of pathogenicity
Variant type
single nucleotide variant
Chromosome / position
2:220286086
Cytoband
2q35
HGVS
NM_001927.4(DES):c.1048C>T (p.Arg350Trp)
Allele change
Missense_R350W

Associated conditions / phenotypes

Primary dilated cardiomyopathy|Desmin-related myofibrillar myopathy|Dilated cardiomyopathy 1I

Public references

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