RS80236571 RET
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Hirschsprung disease
susceptibility to
1
Multiple endocrine neoplasia
type 2
Multiple endocrine neoplasia type 2A
Familial medullary thyroid carcinoma
Multiple endocrine neoplasia type 2B
Pheochromocytoma
Hereditary cancer-predisposing syndrome
Hirschsprung disease
susceptibility to
1
Multiple endocrine neoplasia
type 2
Other Variants in RET