RET, ret proto-oncogene, 5979

N. diseases: 607; N. variants: 162
Disease: Hirschsprung Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2742236
rs2742236
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0019569
Disease:
Hirschsprung Disease 		0.700 GeneticVariation GWASDB Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease. 19196962 2009