RS34682185 RET

Health Risk Chr 10:43106382
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What This Variant Does
"CLNSIG=5
Associated Conditions
Pheochromocytoma
Hirschsprung disease
susceptibility to
1
Renal hypodysplasia/aplasia 1
Multiple endocrine neoplasia
Hereditary cancer-predisposing syndrome
Multiple endocrine neoplasia type 2B
type 2
Hereditary cancer
Multiple endocrine neoplasia type 2A
Pheochromocytoma
Hirschsprung disease
susceptibility to
1
Other Variants in RET
rs76262710 rs75075748 rs75076352 rs75996173 rs79014735 rs80069458 rs79781594 rs77316810 rs77503355 rs77709286
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