RS121908816 TMEM127
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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
Other Variants in TMEM127