PMM2, phosphomannomutase 2, 5373

N. diseases: 214; N. variants: 82
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs28936415
rs28936415
Entrez Id: 5373
Gene Symbol: PMM2
PMM2
CUI: C0007758
Disease:
Cerebellar Ataxia
A 0.700 GeneticVariation CLINVAR
dbSNP: rs28936415
rs28936415
Entrez Id: 5373
Gene Symbol: PMM2
PMM2
CUI: C0007758
Disease:
Cerebellar Ataxia
A 0.700 CausalMutation CLINVAR
dbSNP: rs80338700
rs80338700
Entrez Id: 5373
Gene Symbol: PMM2
PMM2
CUI: C0007758
Disease:
Cerebellar Ataxia
T 0.700 CausalMutation CLINVAR