RS201372601 SDHD
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial complex 2 deficiency
nuclear type 3
Hereditary pheochromocytoma and paraganglioma
Hereditary cancer-predisposing syndrome
Paragangliomas with sensorineural hearing loss
Carney-Stratakis syndrome
Pheochromocytoma
Cowden syndrome 3
Pheochromocytoma/paraganglioma syndrome 1
Mitochondrial complex 2 deficiency
nuclear type 3
Hereditary pheochromocytoma and paraganglioma
Hereditary cancer-predisposing syndrome
Paragangliomas with sensorineural hearing loss
Carney-Stratakis syndrome
Other Variants in SDHD