RS1799939 RET
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What This Variant Does
"rs1799939, also known as Gly691Ser, is a variant in the RET gene. This SNP has been reported to be a...
Associated Conditions
Hereditary cancer-predisposing syndrome
Hirschsprung disease
susceptibility to
1
Renal hypodysplasia/aplasia 1
Multiple endocrine neoplasia
Pheochromocytoma
Multiple endocrine neoplasia type 2A
type 2
Multiple endocrine neoplasia type 2B
Prostate neoplasm
Malignant lymphoma
large B-cell
diffuse
Uterine carcinosarcoma
Other Variants in RET