Variant (rsID / SNP)

rs1801266

rs1801266 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPYD. Location: chromosome 1, position 98,157,332. Clinical significance in the table: drug response.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

DPYDDrug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 1:98157332
Cytoband: 1p21.3
HGVS: NM_000110.4(DPYD):c.703C>T (p.Arg235Trp)
Allele change: Missense_R235W

Associated conditions / phenotypes

Dihydropyrimidine dehydrogenase deficiency|fluorouracil response - Other

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.