CYC1, cytochrome c1, 1537

N. diseases: 44; N. variants: 3
Disease: MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587777042
rs587777042
Entrez Id: 1537
Gene Symbol: CYC1
CYC1
CUI: C3809553
Disease:
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 		0.800 GeneticVariation UNIPROT Mutations in CYC1, encoding cytochrome c1 subunit of respiratory chain complex III, cause insulin-responsive hyperglycemia. 23910460 2013
dbSNP: rs587777042
rs587777042
Entrez Id: 1537
Gene Symbol: CYC1
CYC1
CUI: C3809553
Disease:
MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 6 		T 0.800 CausalMutation CLINVAR