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: rs1864400
rs1864400
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C0019569
Disease:
Hirschsprung Disease
0.700 GeneticVariation GWASCAT A genome-wide association study identifies potential susceptibility loci for Hirschsprung disease. 25310821 2014