RS79890926 RET
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What This Variant Does
"[OMIM:?]
Associated Conditions
MULTIPLE ENDOCRINE NEOPLASIA
TYPE IIA
WITH HIRSCHSPRUNG DISEASE
Multiple endocrine neoplasia
type 2
Hereditary cancer-predisposing syndrome
Multiple endocrine neoplasia
type 2
Hereditary cancer-predisposing syndrome
RET-related disorder
Familial medullary thyroid carcinoma
Hirschsprung disease
susceptibility to
1
Multiple endocrine neoplasia type 2B
Other Variants in RET