Variant (rsID / SNP)
rs62635763
rs62635763 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DES. Location: chromosome 2, position 220,288,509. Clinical significance in the table: Pathogenic/Likely pathogenic.
Reference-table entries
DESPathogenic
- Clinical significance (as recorded)
- Pathogenic/Likely pathogenic
- Variant type
- single nucleotide variant
- Chromosome / position
- 2:220288509
- Cytoband
- 2q35
- HGVS
- NM_001927.4(DES):c.1255C>T (p.Pro419Ser)
- Allele change
- Missense_P419S
Associated conditions / phenotypes
Desmin-related myofibrillar myopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.