CYTB, cytochrome b, 4519

N. diseases: 166; N. variants: 83
Disease: MERRF Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1556424691
rs1556424691
Entrez Id: 4519;4541;4576
Gene Symbol: CYTB;ND6;TRNT
CYTB;ND6;TRNT
CUI: C0162672
Disease:
MERRF Syndrome 		G 0.700 CausalMutation CLINVAR