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Variant (rsID / SNP)

rs55886062

DPYD

rs55886062 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DPYD. Location: chromosome 1, position 97,981,343. 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
1:97981343
Cytoband
1p21.3
HGVS
NM_000110.4(DPYD):c.1679T>G (p.Ile560Ser)
Allele change
Missense_I560S

Associated conditions / phenotypes

Dihydropyrimidine dehydrogenase deficiency|fluorouracil response - Other|capecitabine response - Toxicity|tegafur response - Toxicity|fluorouracil response - Toxicity

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.