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
RS374565577 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hirschsprung disease
RS374893494 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2B
RS375041479 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS375120544 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS375390467 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2B
RS375573788 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia type 2B, Multiple endocrine neoplasia type 2A, Renal hypodysplasia/aplasia 1
RS376565365 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS377130948 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2B
RS377767388 Health Risk Conflicting classifications of pathogenicity Medullary thyroid carcinoma, Multiple endocrine neoplasia, type 2
RS377767390 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS377767392 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia, type 2
RS377767395 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS377767396 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS377767399 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS377767402 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia
RS377767407 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia type 2B, Multiple endocrine neoplasia
RS377767411 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
RS377767416 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS377767417 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia type 2B, Multiple endocrine neoplasia
RS377767420 Health Risk Conflicting classifications of pathogenicity Medullary thyroid carcinoma, Multiple endocrine neoplasia type 2B, Multiple endocrine neoplasia type 2A
RS377767422 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS377767426 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS377767432 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia type 2A, Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia
RS377767433 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia type 2A, Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia
RS386743165 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS527726480 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS527787676 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS529018971 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
RS532810255 Health Risk Conflicting classifications of pathogenicity Pheochromocytoma, Hirschsprung disease, susceptibility to
RS532862288 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
RS534094626 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS536038262 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS536298339 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
RS537523906 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS539995816 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS543376293 Health Risk Conflicting classifications of pathogenicity Pheochromocytoma, Multiple endocrine neoplasia, Renal hypodysplasia/aplasia 1
RS545625150 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS549907428 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS551142665 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS55810667 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hirschsprung disease
RS558718557 Health Risk Conflicting classifications of pathogenicity Renal hypodysplasia/aplasia 1, Pheochromocytoma, Multiple endocrine neoplasia
RS55947360 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS56195026 Health Risk Conflicting classifications of pathogenicity Hereditary cancer-predisposing syndrome, Multiple endocrine neoplasia, type 2
RS566375223 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Multiple endocrine neoplasia type 2A
RS567877611 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS570176656 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
RS572936041 Health Risk Conflicting classifications of pathogenicity Renal hypodysplasia/aplasia 1, Multiple endocrine neoplasia, Hirschsprung disease
RS587778656 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia type 2B, Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia
RS587778659 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia type 2A, Multiple endocrine neoplasia type 2B, Multiple endocrine neoplasia
RS587780809 Health Risk Conflicting classifications of pathogenicity Multiple endocrine neoplasia, type 2, Hereditary cancer-predisposing syndrome
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