CYTB, cytochrome b, 4519

N. diseases: 166; N. variants: 83
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057518882
rs1057518882
Entrez Id: 4519;4540;4541
Gene Symbol: CYTB;ND5;ND6
CYTB;ND5;ND6
CUI: C0456909
Disease:
Blindness
C 0.700 GeneticVariation CLINVAR