RS587781720 SDHA
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary cancer-predisposing syndrome
Pheochromocytoma/paraganglioma syndrome 5
Mitochondrial complex II deficiency
nuclear type 1
Neoplasm of brain
Dilated cardiomyopathy 1GG
Neurodegeneration with ataxia and late-onset optic atrophy
Hereditary cancer-predisposing syndrome
Pheochromocytoma/paraganglioma syndrome 5
Mitochondrial complex II deficiency
nuclear type 1
Neoplasm of brain
Dilated cardiomyopathy 1GG
Neurodegeneration with ataxia and late-onset optic atrophy
Other Variants in SDHA