Source: UNIPROT

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852767
rs137852767
SDHA
CUI: C0023264
Disease: Leigh Disease
Leigh Disease 		0.700 GeneticVariation UNIPROT SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors. 24781757

2015
dbSNP: rs137852767
rs137852767
SDHA
CUI: C0023264
Disease: Leigh Disease
Leigh Disease 		0.700 GeneticVariation UNIPROT Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome. 10746566

2000
dbSNP: rs137852767
rs137852767
SDHA
CUI: C0023264
Disease: Leigh Disease
Leigh Disease 		0.700 GeneticVariation UNIPROT Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency. 7550341

1995