RS151170408 SDHA
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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
Gastrointestinal stromal tumor
Hereditary cancer-predisposing syndrome
Mitochondrial complex II deficiency
nuclear type 1
Pheochromocytoma/paraganglioma syndrome 5
Gastrointestinal stromal tumor
Other Variants in SDHA