MFN2, mitofusin 2, 9927

N. diseases: 334; N. variants: 75
Disease: Hereditary motor and sensory neuropathy with optic atrophy (disorder) ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs119103266
rs119103266
Entrez Id: 9927
Gene Symbol: MFN2
MFN2
CUI: C0393807
Disease:
Hereditary motor and sensory neuropathy with optic atrophy (disorder) 		0.800 GeneticVariation UNIPROT
dbSNP: rs119103266
rs119103266
Entrez Id: 9927
Gene Symbol: MFN2
MFN2
CUI: C0393807
Disease:
Hereditary motor and sensory neuropathy with optic atrophy (disorder) 		T 0.800 CausalMutation CLINVAR