MPO, myeloperoxidase, 4353

N. diseases: 653; N. variants: 25
Disease: Myeloperoxidase Deficiency ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35897051
rs35897051
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0398595
Disease:
Myeloperoxidase Deficiency 		G 0.700 CausalMutation CLINVAR Genetic characterization of myeloperoxidase deficiency in Italy. 15108282 2004
dbSNP: rs35897051
rs35897051
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0398595
Disease:
Myeloperoxidase Deficiency 		G 0.700 CausalMutation CLINVAR Clinical manifestation of myeloperoxidase deficiency. 9766845 1998
dbSNP: rs35897051
rs35897051
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0398595
Disease:
Myeloperoxidase Deficiency 		G 0.700 CausalMutation CLINVAR Hereditary myeloperoxidase deficiency. 6260268 1981