RS75686697 RET
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What This Variant Does
"[OMIM:?]
Associated Conditions
Renal hypodysplasia/aplasia 1
Multiple endocrine neoplasia
type 2
Hereditary cancer-predisposing syndrome
Pheochromocytoma
Hirschsprung disease
susceptibility to
1
Renal hypodysplasia/aplasia 1
Multiple endocrine neoplasia
type 2
Hereditary cancer-predisposing syndrome
Pheochromocytoma
Hirschsprung disease
susceptibility to
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