RS121908816 CIAO1

Health Risk Chr 2:96265261 delins frameshift variant

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What This Variant Does

"[OMIM:?]

Associated Conditions

Pheochromocytoma

Hereditary pheochromocytoma and paraganglioma

Hereditary cancer-predisposing syndrome

TMEM127-related disorder

Inherited phaeochromocytoma and paraganglioma excluding NF1

Pheochromocytoma

Hereditary pheochromocytoma and paraganglioma

Hereditary cancer-predisposing syndrome

TMEM127-related disorder

Inherited phaeochromocytoma and paraganglioma excluding NF1

Population Frequencies

gnomAD ALL

0%

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