RS876658486 SDHA

Health Risk Chr 5:226041
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cancer-predisposing syndrome
Pheochromocytoma/paraganglioma syndrome 5
Mitochondrial complex II deficiency
nuclear type 1
Hereditary cancer-predisposing syndrome
Pheochromocytoma/paraganglioma syndrome 5
Mitochondrial complex II deficiency
nuclear type 1
Other Variants in SDHA
rs9809219 rs137852767 rs1061517 rs137852768 rs387906780 rs151266052 rs142849100 rs587781720 rs587781729 rs80207011
Ask Dr. Hemsworth about this variant