CRBN, cereblon, 51185

N. diseases: 130; N. variants: 16
Disease: Constipation ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0009806
Disease: Constipation
Constipation 		0.010 GeneticVariation phenotype BEFREE The presence of CRBN AA (rs6768972) or TT (rs1672753) genotypes was associated with about 333-fold and 250-fold lower risk of constipation in the course of therapy (OR = 0·003; OR = 0·004, respectively). 31115923 2019