RET, ret proto-oncogene, 5979

N. diseases: 607; N. variants: 162
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2435357
rs2435357
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C3661523
Disease:
Congenital Intestinal Aganglionosis
0.700 GeneticVariation GWASCAT Noncoding RET variants explain the strong association with Hirschsprung disease in patients without rare coding sequence variant. 30031151 2019
dbSNP: rs2505998
rs2505998
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C3661523
Disease:
Congenital Intestinal Aganglionosis
A 0.700 GeneticVariation GWASCAT Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease. 27702942 2016
dbSNP: rs9282834
rs9282834
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C3661523
Disease:
Congenital Intestinal Aganglionosis
A 0.700 GeneticVariation GWASCAT Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease. 27702942 2016
dbSNP: rs1864400
rs1864400
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C3661523
Disease:
Congenital Intestinal Aganglionosis
0.700 GeneticVariation GWASCAT A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease. 25310821 2014
dbSNP: rs2742234
rs2742234
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C3661523
Disease:
Congenital Intestinal Aganglionosis
T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962 2009