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
RS140464432 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS140638866 Health Risk Conflicting classifications of pathogenicity Congenital anomaly of kidney and urinary tract, Multiple endocrine neoplasia, type 2
RS140658743 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2B
RS141016377 Health Risk Conflicting classifications of pathogenicity Renal hypodysplasia/aplasia 1, Multiple endocrine neoplasia, Hirschsprung disease
RS141185224 Health Risk Conflicting classifications of pathogenicity Aganglionic megacolon, Multiple endocrine neoplasia type 2B, Multiple endocrine neoplasia
RS141459368 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS142338976 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS142345108 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS1424549058 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia
RS142641173 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS1427186016 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS142793711 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hirschsprung disease
RS1429462039 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia
RS143948954 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, Renal hypodysplasia/aplasia 1, Hirschsprung disease
RS144192900 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2B
RS144269978 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia type 2B, Multiple endocrine neoplasia type 2A, Pheochromocytoma
RS144730090 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS144981275 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS145122337 Health Risk Conflicting classifications of pathogenicity Pheochromocytoma, Hirschsprung disease, susceptibility to
RS145170911 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2B
RS1453857349 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia
RS145402131 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS145633958 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia type 2A, Hereditary cancer-predisposing syndrome, Aganglionic megacolon
RS145798106 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hirschsprung disease
RS145966037 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS145970248 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS146838520 Health Risk Conflicting classifications of pathogenicity Medullary thyroid carcinoma, Multiple endocrine neoplasia, type 2
RS147219360 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS147437610 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, RET-related disorder
RS147692872 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
RS1478152005 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS1478633054 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Hereditary cancer-predisposing syndrome
RS1480040525 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS1488217326 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS148935214 Health Risk Conflicting classifications of pathogenicity Elevated basal serum calcitonin, Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia type 2A
RS1490617677 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS149238501 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS149252070 Health Risk Conflicting classifications of pathogenicity Pheochromocytoma, Hirschsprung disease, susceptibility to
RS149403911 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Pheochromocytoma
RS149768519 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS149891333 Health Risk Conflicting classifications of pathogenicity Aganglionic megacolon, Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia type 2A
RS149926238 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Renal hypodysplasia/aplasia 1, Hirschsprung disease
RS150261092 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia
RS151148041 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia
RS151267865 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS1554817349 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS1554817395 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS1554817540 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS1554817550 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS1554818529 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
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