RET Chromosome 10

Ret proto-oncogene
508 variants 508 Health Risk

Upload your DNA to see your personal genotypes for variants in RET.

What This Gene Does
This gene encodes a transmembrane receptor and member of the tyrosine protein kinase family of proteins. Binding of ligands such as GDNF (glial cell-line derived neurotrophic factor) and other related proteins to the encoded receptor stimulates receptor dimerization and activation of downstream signaling pathways that play a role in cell differentiation, growth, migration and survival. The encoded receptor is important in development of the nervous system, and the development of organs and tissues derived from the neural crest. This proto-oncogene can undergo oncogenic activation through both cytogenetic rearrangement and activating point mutations. Mutations in this gene are associated with Hirschsprung disease and central hypoventilation syndrome and have been identified in patients with renal agenesis. [provided by RefSeq, Sep 2017]
Gene Info
Gene Group
"Cadherin related|Receptor tyrosine kinases"
Locus Type
gene with protein product
Location
10q11.21
Ensembl
ENSG00000165731
Associated Conditions (57)
Hirschsprung disease
susceptibility to
1
Aganglionic megacolon
Multiple endocrine neoplasia
type 2
Hereditary cancer-predisposing syndrome
Familial medullary thyroid carcinoma
Multiple endocrine neoplasia type 2B
Pheochromocytoma
Multiple endocrine neoplasia type 2A
RET-related disorder
Renal hypodysplasia/aplasia 1
6 conditions
Ovarian cancer
Malignant tumor of breast
Congenital anomaly of kidney and urinary tract
Familial hyperparathyroidism or Hypocalciuric hypercalcaemia
Congenital central hypoventilation
Hereditary cancer
+37 more conditions
Key Variants
RS2435357
Benign; risk factor
Hirschsprung disease, susceptibility to, 1
Health Risk
RS1003057639
Conflicting classifications of pathogenicity
Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
Health Risk
RS1008123818
Conflicting classifications of pathogenicity
Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
Health Risk
RS1013952995
Conflicting classifications of pathogenicity
Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
Health Risk
RS1048022444
Conflicting classifications of pathogenicity
Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
Health Risk
RS1050242868
Conflicting classifications of pathogenicity
Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
Health Risk
RS1060500754
Conflicting classifications of pathogenicity
Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
Health Risk
RS1060500762
Conflicting classifications of pathogenicity
Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
Health Risk
RS113005278
Conflicting classifications of pathogenicity
Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
Health Risk
RS1131691450
Conflicting classifications of pathogenicity
Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia
Health Risk
RS113931414
Conflicting classifications of pathogenicity
Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
Health Risk
RS115272158
Conflicting classifications of pathogenicity
Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
Health Risk
All Variants (508)
RSID Category Clinical Significance Conditions
RS760272063 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hirschsprung disease
RS760625882 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Familial medullary thyroid carcinoma
RS760813493 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS760832715 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS760924186 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS762545740 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
RS762626209 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Pheochromocytoma
RS763296134 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS763489828 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS763617146 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS763670106 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS764938319 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, Hirschsprung disease, susceptibility to
RS765409417 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS765463636 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2B
RS766330880 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS767045208 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS767210575 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
RS767479170 Health Risk Conflicting classifications of pathogenicity Appendicitis, Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia
RS767502292 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS768132465 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
RS768398267 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS768878280 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia
RS769595884 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Renal hypodysplasia/aplasia 1
RS770155054 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS770548816 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS770587835 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia, type 2
RS770637118 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS770736612 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS772292843 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS772684105 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS773256580 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia type 2B, Multiple endocrine neoplasia type 2A
RS773935854 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS774092678 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS774215008 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS774347808 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia type 2B, Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia
RS774474422 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
RS774637214 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS774829203 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia, type 2
RS774983492 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS775086466 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS775114955 Health Risk Conflicting classifications of pathogenicity Renal hypodysplasia/aplasia 1, Multiple endocrine neoplasia, Hirschsprung disease
RS775152474 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS775583354 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
RS775842917 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS775956924 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS776013456 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS776223166 Health Risk Conflicting classifications of pathogenicity Hirschsprung disease, susceptibility to, 1
RS776381183 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS776986585 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS777042445 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
« Prev 1 ... 4 5 6 7 8 9 10 11 Next »
Sign Up to Analyze Your DNA Log In