BCR, BCR activator of RhoGEF and GTPase, 613

N. diseases: 392; N. variants: 7
Disease: Xeroderma Pigmentosum, Complementation Group D ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0268138
Disease: Xeroderma Pigmentosum, Complementation Group D
Xeroderma Pigmentosum, Complementation Group D 		0.010 GeneticVariation disease BEFREE Our results suggest that the XPD Lys751Gln variant genotype increases the risk of CML. 24955348 2014