RS113560320 SDHAF2

Health Risk Chr 11:61437819 snv missense variant
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What This Variant Does
"[OMIM:?]
Associated Conditions
Pheochromocytoma/paraganglioma syndrome 2
Hereditary cancer-predisposing syndrome
Hereditary pheochromocytoma and paraganglioma
Pheochromocytoma/paraganglioma syndrome 2
Hereditary cancer-predisposing syndrome
Hereditary pheochromocytoma and paraganglioma
Other Variants in SDHAF2
rs200911550 rs876658350 rs150187184 rs377266355 rs774508076 rs1060499901 rs1456129845 rs145616631 rs375280597 rs775763888
Ask Dr. Hemsworth about this variant