RS146646971 RET
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What This Variant Does
"CLNSIG=5
Associated Conditions
Multiple endocrine neoplasia type 2A
Multiple endocrine neoplasia
type 2
Hereditary cancer-predisposing syndrome
Familial medullary thyroid carcinoma
Hirschsprung disease
susceptibility to
1
Pheochromocytoma
Multiple endocrine neoplasia type 2B
RET-related disorder
Hereditary cancer-predisposing syndrome
Multiple endocrine neoplasia
type 2
Familial medullary thyroid carcinoma
Other Variants in RET