RS886039439 TMEM127

Health Risk Chr 2:96254061
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary cancer-predisposing syndrome
Hereditary pheochromocytoma and paraganglioma
Pheochromocytoma
Hereditary cancer-predisposing syndrome
Hereditary pheochromocytoma and paraganglioma
Pheochromocytoma
Other Variants in TMEM127
rs121908826 rs121908830 rs121908821 rs121908817 rs121908813 rs121908818 rs121908822 rs121908814 rs121908825 rs121908827
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