Variant (rsID / SNP)

rs28371725

rs28371725 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CYP2D6. Location: chromosome 22, position 42,523,805. Clinical significance in the table: Likely benign; drug response; other.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

CYP2D6Likely benign

Clinical significance (as recorded): Likely benign; drug response; other
Variant type: single nucleotide variant
Chromosome / position: 22:42523805
Cytoband: 22q13.2
HGVS: CYP2D6*41
Allele change: Silent

Associated conditions / phenotypes

Tramadol response|Deutetrabenazine response|Tamoxifen response

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.