RS9282835 RET

Health Risk Chr 10:43111201 snv splice region variant

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Associated Conditions

Multiple endocrine neoplasia

type 2

Hirschsprung disease

susceptibility to

Hereditary cancer-predisposing syndrome

Multiple endocrine neoplasia type 2B

Hirschsprung disease

susceptibility to

Familial medullary thyroid carcinoma

Multiple endocrine neoplasia type 2A

Pheochromocytoma

Multiple endocrine neoplasia

type 2

Population Frequencies

gnomAD ALL

99.6%

1kG AFR

10%

1kG ALL

97%

1kG AMR

97.8%

1kG EAS

100%

1kG EUR

99.7%

1kG SAS

100%

Other Variants in RET