RS397514034 SDHD
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What This Variant Does
"CLNSIG=5
Associated Conditions
Pheochromocytoma/paraganglioma syndrome 1
Hereditary cancer-predisposing syndrome
Paragangliomas with sensorineural hearing loss
Cowden syndrome 3
Carney-Stratakis syndrome
Pheochromocytoma
Mitochondrial complex 2 deficiency
nuclear type 3
Hereditary pheochromocytoma and paraganglioma
Pheochromocytoma/paraganglioma syndrome 1
Hereditary cancer-predisposing syndrome
Paragangliomas with sensorineural hearing loss
Cowden syndrome 3
Carney-Stratakis syndrome
Pheochromocytoma
Other Variants in SDHD