RS34779890 SDHA
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Associated Conditions
Mitochondrial complex II deficiency
nuclear type 1
Pheochromocytoma/paraganglioma syndrome 5
Hereditary cancer-predisposing syndrome
Hereditary pheochromocytoma and paraganglioma
Leigh syndrome
SDHA-related disorder
Neurodegeneration with ataxia and late-onset optic atrophy
Dilated cardiomyopathy 1GG
Mitochondrial complex II deficiency
nuclear type 1
Pheochromocytoma/paraganglioma syndrome 5
Hereditary cancer-predisposing syndrome
Hereditary pheochromocytoma and paraganglioma
Leigh syndrome
Other Variants in SDHA