DPYD, dihydropyrimidine dehydrogenase, 1806

N. diseases: 249; N. variants: 101
Disease: Dihydropyrimidine Dehydrogenase Deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72549310
rs72549310
Entrez Id: 1806
Gene Symbol: DPYD
DPYD
CUI: C1959620
Disease:
Dihydropyrimidine Dehydrogenase Deficiency 		A 0.700 GeneticVariation CLINVAR Comparative functional analysis of DPYD variants of potential clinical relevance to dihydropyrimidine dehydrogenase activity. 24648345 2014
dbSNP: rs72549310
rs72549310
Entrez Id: 1806
Gene Symbol: DPYD
DPYD
CUI: C1959620
Disease:
Dihydropyrimidine Dehydrogenase Deficiency 		A 0.700 GeneticVariation CLINVAR Clinical relevance of different dihydropyrimidine dehydrogenase gene single nucleotide polymorphisms on 5-fluorouracil tolerance. 17121937 2006
dbSNP: rs72549310
rs72549310
Entrez Id: 1806
Gene Symbol: DPYD
DPYD
CUI: C1959620
Disease:
Dihydropyrimidine Dehydrogenase Deficiency 		A 0.700 GeneticVariation CLINVAR Lethal 5-fluorouracil toxicity associated with a novel mutation in the dihydropyrimidine dehydrogenase gene. 12562666 2003