Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs377022708
rs377022708
Entrez Id: 28976;57501
Gene Symbol: ACAD9;KIAA1257
ACAD9;KIAA1257
CUI: C4747517
Disease:
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20 		0.800 GeneticVariation UNIPROT
dbSNP: rs377022708
rs377022708
Entrez Id: 28976;57501
Gene Symbol: ACAD9;KIAA1257
ACAD9;KIAA1257
CUI: C4747517
Disease:
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20 		T 0.800 CausalMutation CLINVAR