RS778207102 SDHA
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Associated Conditions
Pheochromocytoma/paraganglioma syndrome 5
Mitochondrial complex II deficiency
nuclear type 1
Hereditary cancer-predisposing syndrome
SDHA-related disorder
Neurodegeneration with ataxia and late-onset optic atrophy
Dilated cardiomyopathy 1GG
Pheochromocytoma/paraganglioma syndrome 5
Mitochondrial complex II deficiency
nuclear type 1
Hereditary cancer-predisposing syndrome
SDHA-related disorder
Neurodegeneration with ataxia and late-onset optic atrophy
Dilated cardiomyopathy 1GG
Other Variants in SDHA