rs1801160
A SNP in the DPYD gene on chromosome 1. Its most notable genotype is T;T: 5-fluorouracil toxicity (?)
- Gene
- DPYD
- Location
- Chr 197,305,364 (GRCh38)
- Highest magnitude
- 3.5Important
- Tested on
- 23andMe, AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TMost notableBad5-fluorouracil toxicity (?)
- C;TBadPossible 5-fluorouracil toxicity
- C;CGoodcommon/normal
SNPedia records rs1801160 on the minus strand: (A;A), (A;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Conditions, medicines and genes
Other DPYD SNPs
- rs3918290T;T5-fluorouracil toxicity, dihydropyrimidine dehydrogenase deficiencyImportant
- rs55886062C;C5-fluorouracil toxicityImportant
- rs67376798A;A5-fluorouracil toxicityImportant
- rs1801159T;Tcommon in clinvarTypical
- rs1801265G;Gcommon in clinvarTypical
- rs1801268C;Ccommon genotypeTypical
- rs2297595T;Tcommon on affy axiom dataTypical
Notes
From SNPedia
Notes
rs1801160, also known as V732I or p.Val732Ile, is a variant in the DPYD gene on chromosome 1. A pharmacogenetic study of ~1,500 colon cancer patients treated with a 5-fluorouracil regimen concluded that patients with a rs1801160(A) allele were at roughly a 2-fold higher risk for an adverse effect (from the fluorouracil). The absolute frequencies of the various adverse effects varied; for example, neutropenia occurred in about 1 in 10 patients (so about 1 in 5 rs1801160(A) carriers).
Source and license
Adapted from rs1801160 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.