RS78014899 RET
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What This Variant Does
"[OMIM:?]
Associated Conditions
Familial medullary thyroid carcinoma
Multiple endocrine neoplasia
type 2
Hereditary cancer-predisposing syndrome
Hepatocellular carcinoma
Multiple endocrine neoplasia
type 2
Multiple endocrine neoplasia type 2B
Multiple endocrine neoplasia type 2A
Hereditary cancer-predisposing syndrome
MEN2 phenotype: Unclassified
Familial medullary thyroid carcinoma
Multiple endocrine neoplasia
type 2
Hereditary cancer-predisposing syndrome
Other Variants in RET