Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907272
rs387907272
MYD88
CUI: C0598766
Disease: Leukemogenesis
Leukemogenesis 		0.020 GeneticVariation BEFREE Genetically, PA-DLBCL harbored a high prevalence of MYD88 L265P (24%) and CD79B mutations (52%) which may be involved in lymphomagenesis. 31609782

2020
dbSNP: rs387907272
rs387907272
MYD88
CUI: C0598766
Disease: Leukemogenesis
Leukemogenesis 		0.020 GeneticVariation BEFREE In order to evaluate whether the presence of the recently described MYD88 L265P mutation in patients with Waldenström's macroglobulinemia (WM) is contributory to SS-associated lymphomagenesis, a quantitative allele-specific PCR method was performed in peripheral blood derived from 90 SS patients as well as in minor salivary gland tissues derived from 12 primary SS patients with or without lymphoma. 24153350

2014