RS766667009 SDHA

Health Risk Chr 5:251104
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cancer-predisposing syndrome
Mitochondrial complex II deficiency
nuclear type 1
Pheochromocytoma/paraganglioma syndrome 5
Neurodegeneration with ataxia and late-onset optic atrophy
Dilated cardiomyopathy 1GG
Pheochromocytoma/paraganglioma syndrome 5
Mitochondrial complex II deficiency
nuclear type 1
Dilated cardiomyopathy 1GG
Neurodegeneration with ataxia and late-onset optic atrophy
Hereditary cancer-predisposing syndrome
Mitochondrial complex II deficiency
nuclear type 1
Pheochromocytoma/paraganglioma syndrome 5
Other Variants in SDHA
rs9809219 rs137852767 rs1061517 rs137852768 rs387906780 rs151266052 rs142849100 rs587781720 rs587781729 rs80207011
Ask Dr. Hemsworth about this variant