RS9809219 SDHA
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What This Variant Does
"[OMIM:?]
Associated Conditions
Mitochondrial complex II deficiency
nuclear type 1
Pheochromocytoma/paraganglioma syndrome 5
Hereditary cancer-predisposing syndrome
Leigh syndrome
Diffuse midline glioma
H3 K27-altered
Dilated cardiomyopathy 1GG
Neurodegeneration with ataxia and late-onset optic atrophy
SDHA-related disorder
Cardiac arrhythmia
Mitochondrial complex II deficiency
nuclear type 1
Pheochromocytoma/paraganglioma syndrome 5
Hereditary cancer-predisposing syndrome
Other Variants in SDHA