RS17158558 RET
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What This Variant Does
"A complex pattern of mutations involving rs17158558(T) and other mutations simultaneously occurring ...
Associated Conditions
Hirschsprung disease
susceptibility to
1
Hereditary cancer-predisposing syndrome
Multiple endocrine neoplasia
Renal hypodysplasia/aplasia 1
Familial medullary thyroid carcinoma
Multiple endocrine neoplasia type 2B
Pheochromocytoma
Multiple endocrine neoplasia type 2A
Aganglionic megacolon
type 2
Malignant tumor of breast
Breast-ovarian cancer
familial
Other Variants in RET