RS587782243 SDHB

Health Risk Chr 1:17033060
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary cancer-predisposing syndrome
Pheochromocytoma/paraganglioma syndrome 4
Gastrointestinal stromal tumor
Pheochromocytoma
Hereditary pheochromocytoma and paraganglioma
Melanoma
Inherited phaeochromocytoma and paraganglioma excluding NF1
Gastrointestinal stromal tumor
Pheochromocytoma/paraganglioma syndrome 4
Pheochromocytoma
Hereditary pheochromocytoma and paraganglioma
Hereditary cancer-predisposing syndrome
Pheochromocytoma/paraganglioma syndrome 4
Gastrointestinal stromal tumor
Pheochromocytoma
Other Variants in SDHB
rs74315366 rs74315367 rs74315368 rs587781266 rs74315369 rs74315370 rs74315371 rs74315372 rs121917755 rs398122805
Ask Dr. Hemsworth about this variant