RS202198133 SDHD
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What This Variant Does
"CLNSIG=5
Associated Conditions
Mitochondrial complex 2 deficiency
nuclear type 3
Mitochondrial complex II deficiency
nuclear type 1
Hereditary cancer-predisposing syndrome
Paragangliomas with sensorineural hearing loss
Carney-Stratakis syndrome
Pheochromocytoma
Cowden syndrome 3
SDHD-related disorder
Carney-Stratakis syndrome
Pheochromocytoma
Paragangliomas with sensorineural hearing loss
Cowden syndrome 3
Mitochondrial complex 2 deficiency
Other Variants in SDHD