RS587776649 SDHD
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What This Variant Does
"CLNSIG=5
Associated Conditions
Carney-Stratakis syndrome
Hereditary cancer-predisposing syndrome
Hereditary pheochromocytoma and paraganglioma
Paragangliomas with sensorineural hearing loss
Pheochromocytoma
Cowden syndrome 3
Mitochondrial complex 2 deficiency
nuclear type 3
Pheochromocytoma/paraganglioma syndrome 1
Inherited phaeochromocytoma and paraganglioma excluding NF1
Carney-Stratakis syndrome
Hereditary cancer-predisposing syndrome
Hereditary pheochromocytoma and paraganglioma
Paragangliomas with sensorineural hearing loss
Pheochromocytoma
Other Variants in SDHD