CYTB, cytochrome b, 4519

N. diseases: 166; N. variants: 83
Disease: Optic Atrophy, Hereditary, Leber ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs200336777
rs200336777
Entrez Id: 4519;4541
Gene Symbol: CYTB;ND6
CYTB;ND6
CUI: C0917796
Disease:
Optic Atrophy, Hereditary, Leber 		0.700 GeneticVariation UNIPROT