RS75996173 RET
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What This Variant Does
"[OMIM:?]
Associated Conditions
Multiple endocrine neoplasia type 2A
Pheochromocytoma
Hereditary cancer-predisposing syndrome
Multiple endocrine neoplasia type 2B
Multiple endocrine neoplasia
type 2
Hirschsprung disease
susceptibility to
1
RET-related disorder
Familial medullary thyroid carcinoma
Multiple endocrine neoplasia type 2A
Pheochromocytoma
Multiple endocrine neoplasia
type 2
Other Variants in RET