RS77724903 RET
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What This Variant Does
"[OMIM:?]
Associated Conditions
Pheochromocytoma
Familial medullary thyroid carcinoma
Hereditary cancer-predisposing syndrome
Aganglionic megacolon
Hirschsprung disease
susceptibility to
1
Multiple endocrine neoplasia
Renal hypodysplasia/aplasia 1
Multiple endocrine neoplasia type 2A
Multiple endocrine neoplasia type 2B
Familial cancer of breast
type 2
Pheochromocytoma
Familial medullary thyroid carcinoma
Other Variants in RET