Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907272
rs387907272
0.040 GeneticVariation BEFREE The MYD88 L265P mutation may play a key role in the pathogenesis of IgM monoclonal gammopathies. 28280994

2017

dbSNP: rs387907272
rs387907272
0.040 GeneticVariation BEFREE MYD88 L265P mutation has been reported in ∼90% of Waldenström's Macroglobulinemia (WM) patients and immunoglobulin M (IgM) monoclonal gammopathies of uncertain significance (MGUS), as well as in some cases of lymphoma and chronic lymphocytic leukemia. 24992174

2015

dbSNP: rs387907272
rs387907272
0.040 GeneticVariation BEFREE MYD88 L265P is highly prevalent in Waldenstrom's Macroglobulinemia (WM) and IgM monoclonal gammopathy of unknown significance (MGUS). 24509637

2014

dbSNP: rs387907272
rs387907272
0.040 GeneticVariation BEFREE MYD88 L265P was absent in paired normal tissue samples from patients with Waldenström's macroglobulinemia or non-IgM LPL and in B cells from healthy donors and was absent or rarely expressed in samples from patients with multiple myeloma, marginal-zone lymphoma, or IgM monoclonal gammopathy of unknown significance. 22931316

2012