Variant (rsID / SNP)
rs67376798
rs67376798 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPYD. Location: chromosome 1, position 97,547,947. Clinical significance in the table: drug response.
Reference-table entries
DPYDDrug response
- Clinical significance (as recorded)
- drug response
- Variant type
- single nucleotide variant
- Chromosome / position
- 1:97547947
- Cytoband
- 1p21.3
- HGVS
- NM_000110.4(DPYD):c.2846A>T (p.Asp949Val)
- Allele change
- Missense_D949V
Associated conditions / phenotypes
Dihydropyrimidine dehydrogenase deficiency|Fluorouracil response|Inborn genetic diseases|tegafur response - Toxicity|capecitabine response - Toxicity|fluorouracil response - Toxicity|fluorouracil response - Other
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.