Variant (rsID / SNP)

rs1801268

rs1801268 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPYD. Location: chromosome 1, position 97,544,627. Clinical significance in the table: drug response.

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Reference-table entries

DPYDDrug response

Clinical significance (as recorded): drug response
Variant type: single nucleotide variant
Chromosome / position: 1:97544627
Cytoband: 1p21.3
HGVS: NM_000110.4(DPYD):c.2983G>T (p.Val995Phe)
Allele change: Missense_V995F

Associated conditions / phenotypes

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.