RS786202100 SDHB
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cancer-predisposing syndrome
Pheochromocytoma
Gastrointestinal stromal tumor
Pheochromocytoma/paraganglioma syndrome 4
Mitochondrial complex 2 deficiency
nuclear type 4
Carney-Stratakis syndrome
SDHB-related disorder
Hereditary cancer-predisposing syndrome
Pheochromocytoma
Gastrointestinal stromal tumor
Pheochromocytoma/paraganglioma syndrome 4
Mitochondrial complex 2 deficiency
nuclear type 4
Carney-Stratakis syndrome
Other Variants in SDHB