RET Chromosome 10

Ret proto-oncogene
508 variants 508 Health Risk

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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
RS200956659 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS201030628 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS201244749 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS201550433 Health Risk Conflicting classifications of pathogenicity Renal hypodysplasia/aplasia 1, Hirschsprung disease, susceptibility to
RS201553718 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Medullary thyroid carcinoma
RS201740483 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia type 2A, Ewing sarcoma of soft tissue
RS201745826 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia
RS201816539 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS201992974 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
RS2132658120 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS2132663101 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS2132678154 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS2132678531 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Ovarian cancer
RS2132709323 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS2132721114 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS2132746693 Health Risk Conflicting classifications of pathogenicity Familial medullary thyroid carcinoma, Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia
RS2132766849 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS2132767932 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS2132776895 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS2132813703 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS2132847951 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS2132856009 Health Risk Conflicting classifications of pathogenicity Hirschsprung disease, susceptibility to, 1
RS2132987446 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia
RS2133006493 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS2133032257 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS2133037467 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS2491932875 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS2492157382 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS2538403940 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS2538580125 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
RS2538625661 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia
RS267607011 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia type 2A, Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia type 2A
RS34617196 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2B
RS34682185 Health Risk Conflicting classifications of pathogenicity Pheochromocytoma, Hirschsprung disease, susceptibility to
RS367737920 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
RS368137511 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
RS368550200 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, 6 conditions
RS369116900 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS369152977 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS369579749 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2B
RS369769303 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia, type 2
RS370736139 Health Risk Conflicting classifications of pathogenicity Aganglionic megacolon, Multiple endocrine neoplasia, type 2
RS371153966 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS371731991 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS372191563 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS372648203 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS372673589 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS373540097 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia
RS373594744 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS374461212 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
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