RS75234356 RET
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What This Variant Does
"[OMIM:?]
Associated Conditions
Multiple endocrine neoplasia type 2A
Familial medullary thyroid carcinoma
Multiple endocrine neoplasia
type 2
Multiple endocrine neoplasia type 2B
Hereditary cancer-predisposing syndrome
MEN2 phenotype: Unclassified
Hirschsprung disease
susceptibility to
1
Pheochromocytoma
Multiple endocrine neoplasia II
Medullary thyroid carcinoma
RET-related disorder
Multiple endocrine neoplasia type 2A
Other Variants in RET