rs1805794, NBN

N. diseases: 41
Disease: Hodgkin Disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Hodgkin Disease
CUI: C0019829
Disease: Hodgkin Disease
0.010 GeneticVariation BEFREE We observed that, in combination, allelic variants in the XPC Ala499Val, NBN Glu185Gln, XRCC3 Thr241Me, XRCC1 Arg194Trp, and XRCC1 399Gln polymorphisms modify the risk for developing HL. 21374732 2011