Variant (rsID / SNP)
rs985861
rs985861 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSC1. Location: chromosome 18, position 28,710,619. The table records no clinical significance for this variant.
Reference-table entries
DSC1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 18:28710619
- HGVS
- NM_024421.2,c.2543G>T,p.Cys848Phe
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.