RS786203457 SDHC

Health Risk Chr 1:161356815
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary cancer-predisposing syndrome
Pheochromocytoma/paraganglioma syndrome 3
Gastrointestinal stromal tumor
Hereditary pheochromocytoma and paraganglioma
Inherited phaeochromocytoma and paraganglioma excluding NF1
Hereditary cancer-predisposing syndrome
Pheochromocytoma/paraganglioma syndrome 3
Gastrointestinal stromal tumor
Hereditary pheochromocytoma and paraganglioma
Inherited phaeochromocytoma and paraganglioma excluding NF1
Other Variants in SDHC
rs587776652 rs587776653 rs201210474 rs201286421 rs587778661 rs786202200 rs786202080 rs764575966 rs200375156 rs786205146
Ask Dr. Hemsworth about this variant