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: rs119468010
rs119468010
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0398595
Disease:
Myeloperoxidase Deficiency 		0.810 GeneticVariation BEFREE We recently identified a missense mutation, R569W, in the MPO gene of many subjects with MPO deficiency. 8621627 1996
dbSNP: rs119468010
rs119468010
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0398595
Disease:
Myeloperoxidase Deficiency 		A 0.810 CausalMutation CLINVAR
dbSNP: rs119468010
rs119468010
Entrez Id: 4353
Gene Symbol: MPO
MPO
CUI: C0398595
Disease:
Myeloperoxidase Deficiency 		0.810 GeneticVariation UNIPROT