RS397516836 SDHB
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary pheochromocytoma and paraganglioma
Hereditary cancer-predisposing syndrome
Pheochromocytoma/paraganglioma syndrome 4
Pheochromocytoma
Gastrointestinal stromal tumor
Hereditary cancer-predisposing syndrome
Pheochromocytoma
Gastrointestinal stromal tumor
Pheochromocytoma/paraganglioma syndrome 4
Hereditary pheochromocytoma and paraganglioma
Mitochondrial complex 2 deficiency
nuclear type 4
Carney-Stratakis syndrome
Inherited phaeochromocytoma and paraganglioma excluding NF1
Hereditary pheochromocytoma and paraganglioma
Other Variants in SDHB