Source: UNIPROT ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906780
rs387906780
Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C3279992
Disease:
PARAGANGLIOMAS 5 		0.800 GeneticVariation UNIPROT Pheochromocytoma and paraganglioma: an endocrine society clinical practice guideline. 24893135 2014
dbSNP: rs137852768
rs137852768
Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C3150898
Disease:
CARDIOMYOPATHY, DILATED, 1GG 		0.800 GeneticVariation UNIPROT Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase. 20551992 2010
dbSNP: rs387906780
rs387906780
Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C3279992
Disease:
PARAGANGLIOMAS 5 		0.800 GeneticVariation UNIPROT SDHA is a tumor suppressor gene causing paraganglioma. 20484225 2010
dbSNP: rs137852768
rs137852768
Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C1855008
Disease:
Mitochondrial Complex II Deficiency 		0.800 GeneticVariation UNIPROT
dbSNP: rs137852767
rs137852767
Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C0023264
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
Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C0023264
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
Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C0023264
Disease:
Leigh Disease 		0.700 GeneticVariation UNIPROT Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency. 7550341 1995
dbSNP: rs9809219
rs9809219
Entrez Id: 6389
Gene Symbol: SDHA
SDHA
CUI: C0023264
Disease:
Leigh Disease 		0.700 GeneticVariation UNIPROT