Variant (rsID / SNP)
rs786204293
rs786204293 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DSP. Location: chromosome 6, position 7,568,695. The table records no clinical significance for this variant.
Reference-table entries
DSPNot classified
- Variant type
- Duplication
- Chromosome / position
- 6:7568695
- Cytoband
- 6p24.3
- HGVS
- NM_004415.4(DSP):c.1292dup (p.Tyr431Ter)
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.