CYTB, cytochrome b, 4519

N. diseases: 166; N. variants: 83
Disease: MERFF SYNDROME ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199474701
rs199474701
Entrez Id: 4519;4541;4571
Gene Symbol: CYTB;ND6;TRNP
CYTB;ND6;TRNP
CUI: C4016625
Disease:
MERFF SYNDROME 		A 0.700 CausalMutation CLINVAR