Variant (rsID / SNP)

rs776786349

rs776786349 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DES. Location: chromosome 2, position 220,286,218. 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: 2:220286218
Cytoband: 2q35
HGVS: NM_001927.4(DES):c.1180G>A (p.Val394Met)
Allele change: Missense_V394M

Associated conditions / phenotypes

Cardiomyopathy|Desmin-related myofibrillar myopathy

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.