DPYS, dihydropyrimidinase, 1807

N. diseases: 63; N. variants: 8
Disease: Dihydropyrimidinase deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606773
rs267606773
Entrez Id: 1807
Gene Symbol: DPYS
DPYS
CUI: C0342803
Disease:
Dihydropyrimidinase deficiency 		0.800 GeneticVariation UNIPROT Clinical genetics evaluation in identifying the etiology of autism spectrum disorders: 2013 guideline revisions. 23519317 2013
dbSNP: rs267606773
rs267606773
Entrez Id: 1807
Gene Symbol: DPYS
DPYS
CUI: C0342803
Disease:
Dihydropyrimidinase deficiency 		0.800 GeneticVariation UNIPROT Dihydropyrimidinase deficiency: structural organization, chromosomal localization, and mutation analysis of the human dihydropyrimidinase gene. 9718352 1998
dbSNP: rs267606773
rs267606773
Entrez Id: 1807
Gene Symbol: DPYS
DPYS
CUI: C0342803
Disease:
Dihydropyrimidinase deficiency 		T 0.800 CausalMutation CLINVAR