RS377470390 SDHA
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Associated Conditions
Pheochromocytoma/paraganglioma syndrome 5
Mitochondrial complex II deficiency
nuclear type 1
Hereditary cancer-predisposing syndrome
Leigh syndrome
Dilated cardiomyopathy 1GG
Diffuse pediatric-type high-grade glioma
H3-wildtype and IDH-wildtype
Neurodegeneration with ataxia and late-onset optic atrophy
Pheochromocytoma/paraganglioma syndrome 5
Mitochondrial complex II deficiency
nuclear type 1
Hereditary cancer-predisposing syndrome
Leigh syndrome
Dilated cardiomyopathy 1GG
Other Variants in SDHA