Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Waldenstrom Macroglobulinemia
CUI: C0024419
Disease: Waldenstrom Macroglobulinemia
0.010 GeneticVariation BEFREE The MYD88 L265P mutation is present in nearly 90% of patients with Waldenström macroglobulinemia. 30190015 2018