RS367721665 SDHA

Health Risk Chr 5:230935
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Associated Conditions
Skeletal myopathy
Mitochondrial complex II deficiency
nuclear type 1
Pheochromocytoma/paraganglioma syndrome 5
Hereditary pheochromocytoma and paraganglioma
Leigh syndrome
Hereditary cancer-predisposing syndrome
Dilated cardiomyopathy 1GG
Neurodegeneration with ataxia and late-onset optic atrophy
Skeletal myopathy
Mitochondrial complex II deficiency
nuclear type 1
Pheochromocytoma/paraganglioma syndrome 5
Hereditary pheochromocytoma and paraganglioma
Leigh syndrome
Other Variants in SDHA
rs9809219 rs137852767 rs1061517 rs137852768 rs387906780 rs151266052 rs142849100 rs587781720 rs587781729 rs80207011
Ask Dr. Hemsworth about this variant