Variant (rsID / SNP)
rs730882170
rs730882170 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2D6. Location: chromosome 22, position 42,523,848. Clinical significance in the table: drug response.
Reference-table entries
CYP2D6Drug response
- Clinical significance (as recorded)
- drug response
- Variant type
- Deletion
- Chromosome / position
- 22:42523848
- Cytoband
- 22q13.2
- HGVS
- NM_000106.6(CYP2D6):c.963_981del (p.Met321fs)
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.