RS886041237 SDHD
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cancer-predisposing syndrome
Hereditary pheochromocytoma and paraganglioma
Pheochromocytoma
Carney-Stratakis syndrome
Paragangliomas with sensorineural hearing loss
Cowden syndrome 3
Hereditary cancer-predisposing syndrome
Hereditary pheochromocytoma and paraganglioma
Pheochromocytoma
Carney-Stratakis syndrome
Paragangliomas with sensorineural hearing loss
Cowden syndrome 3
Other Variants in SDHD