RS79658334 RET
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What This Variant Does
"[OMIM:?]
Associated Conditions
Multiple endocrine neoplasia
type 2
Hereditary cancer-predisposing syndrome
7 conditions
MEN2 phenotype: Unclassified
Multiple endocrine neoplasia type 2A
Familial medullary thyroid carcinoma
Hirschsprung disease
susceptibility to
1
Ovarian cancer
RET-related disorder
Multiple endocrine neoplasia type 2B
Pheochromocytoma
Inherited phaeochromocytoma and paraganglioma excluding NF1
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