RS587778661 SDHC

Health Risk Chr 1:161328466
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary cancer-predisposing syndrome
Gastrointestinal stromal tumor
Pheochromocytoma/paraganglioma syndrome 3
Hereditary pheochromocytoma and paraganglioma
Hereditary cancer-predisposing syndrome
Gastrointestinal stromal tumor
Pheochromocytoma/paraganglioma syndrome 3
Hereditary pheochromocytoma and paraganglioma
Other Variants in SDHC
rs587776652 rs587776653 rs201210474 rs201286421 rs786202200 rs786202080 rs786203457 rs764575966 rs200375156 rs786205146
Ask Dr. Hemsworth about this variant