RET, ret proto-oncogene, 5979

N. diseases: 607; N. variants: 162
Disease: Congenital central hypoventilation ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs192489011
rs192489011
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1275808
Disease:
Congenital central hypoventilation 		0.700 GeneticVariation UNIPROT