RS138624658 RET

Health Risk Chr 10:43111366 snv missense variant
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Associated Conditions
Aganglionic megacolon
Multiple endocrine neoplasia
type 2
Hereditary cancer-predisposing syndrome
Hirschsprung disease
susceptibility to
1
Pheochromocytoma
Multiple endocrine neoplasia type 2A
Familial medullary thyroid carcinoma
Multiple endocrine neoplasia type 2B
Aganglionic megacolon
Multiple endocrine neoplasia
type 2
Hereditary cancer-predisposing syndrome
Population Frequencies
gnomAD ALL
100%
Other Variants in RET
rs76262710 rs75075748 rs75076352 rs75996173 rs79014735 rs80069458 rs79781594 rs77316810 rs77503355 rs77709286
Ask Dr. Hemsworth about this variant