Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1801265
rs1801265
DPYD
0.710 GeneticVariation BEFREE This analysis identified the variants c.85T>C and c.496A>G, which were previously described as pivotal components of the haplotype associated with decreased enzyme activity and suggested that both variant alleles are related to DPD deficiency. 30915274

2019
dbSNP: rs1801265
rs1801265
DPYD
0.710 GeneticVariation UNIPROT