Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs35897051
rs35897051
MPO
CUI: C0398595
Disease: Myeloperoxidase Deficiency
Myeloperoxidase Deficiency 		G 0.700 CausalMutation CLINVAR Genetic characterization of myeloperoxidase deficiency in Italy. 15108282

2004
dbSNP: rs35897051
rs35897051
MPO
CUI: C0398595
Disease: Myeloperoxidase Deficiency
Myeloperoxidase Deficiency 		G 0.700 CausalMutation CLINVAR Clinical manifestation of myeloperoxidase deficiency. 9766845

1998
dbSNP: rs35897051
rs35897051
MPO
CUI: C0398595
Disease: Myeloperoxidase Deficiency
Myeloperoxidase Deficiency 		G 0.700 CausalMutation CLINVAR Hereditary myeloperoxidase deficiency. 6260268

1981