Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE Four cases of small lymphocyte-predominant benign PE from patients without history of lymphoma were examined and were all negative for MYD88 L265P mutation. 31556196

2019

dbSNP: rs2230926
rs2230926
0.040 GeneticVariation BEFREE However, the rs2230926 variant allele seems to confer a higher risk to develop lymphoma in pSS patients, while in RA patients, the presence of RF resulted significantly associated with the variant allele. 31534975

2019

dbSNP: rs121913503
rs121913503
0.010 GeneticVariation BEFREE The test evaluates the expression of 20 genes, including 17 markers relevant to T-cell immunology and lymphoma biopathology, one EBV-related transcript, and variants of RHOA (G17V) and IDH2 (R172K/T). 31488561

2019

dbSNP: rs1353428252
rs1353428252
0.010 GeneticVariation BEFREE The test evaluates the expression of 20 genes, including 17 markers relevant to T-cell immunology and lymphoma biopathology, one EBV-related transcript, and variants of RHOA (G17V) and IDH2 (R172K/T). 31488561

2019

dbSNP: rs1057519781
rs1057519781
ALK
0.010 GeneticVariation BEFREE Activation of IGF-1R pathway and NPM-ALK G1269A mutation confer resistance to crizotinib treatment in NPM-ALK positive lymphoma. 31177400

2019

dbSNP: rs3099844
rs3099844
0.010 GeneticVariation BEFREE <i>HCP5</i> rs3099844 was associated with anti-SSA (<i>P</i> = 0.006, OR = 3.07) and anti-SSB (<i>P</i> = 0.005, OR = 2.66) antibodies, severity of focus score (<i>P</i> = 0.03, OR = 12), and lymphoma development (<i>P</i> = 0.002, OR = 7.23). 30882006

2019

dbSNP: rs2230926
rs2230926
0.040 GeneticVariation BEFREE Increased prevalence of the rs2230926 mutant variant was detected in both SS-lymphoma and SS-nonlymphoma subgroups compared to HC (8.8% vs. 7.6% vs. 3.6%, <i>p</i> values: 0.04 and 0.03, respectively) in association with higher IgM, LDH serum levels, and PB <i>Bcl-XL</i> transcripts but lower leucocyte and neutrophil counts. 30662920

2018

dbSNP: rs138228187
rs138228187
0.010 GeneticVariation BEFREE TIRAP p.R81C is a novel lymphoma risk variant which enhances cell proliferation <i>via</i> NF-κB mediated signaling in B-cells. 30381301

2019

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE Suppressing IL-10 significantly reduced STAT3 activation in both MYD88 WT and MYD88 L265P m</spa</span>n>utant lymphomas</span>. 30253331

2018

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE MYD88 L265P MUTATION DETECTION IN THE AQUEOUS HUMOR OF PATIENTS WITH VITREORETINAL LYMPHOMA. 30204732

2019

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE With clinical trials regarding their efficacy rapidly expanding to NHLs, we also discuss potential combinations of immune checkpoint inhibitors with the described targeted chemotherapies of L265P signaling networks, and/or with the above immunological approaches as potential ways of targeting MYD88-mutated lymphomas in the future. 30203262

2018

dbSNP: rs2231231
rs2231231
0.010 GeneticVariation BEFREE Accordingly, we analyzed the association between a single-nucleotide polymorphism locus of aquaporin 3 (rs2231231) and Epstein-Barr virus (EBV)-associated nasopharyngeal carcinoma (EBVaNPC), lymphoma (EBVaL), and gastric carcinoma in China. 30110699

2018

dbSNP: rs1946518
rs1946518
0.010 GeneticVariation BEFREE We found that IL-18 (rs1946518) and NFκB94 ins/del (rs28362491) contributed to lymphoma susceptibility and allele G in IL-18 was significantly associated with the risk of lymphoma. 29312552

2017

dbSNP: rs28362491
rs28362491
0.010 GeneticVariation BEFREE We found that IL-18 (rs1946518) and NFκB94 ins/del (rs28362491) contributed to lymphoma susceptibility and allele G in IL-18 was significantly associated with the risk of lymphoma. 29312552

2017

dbSNP: rs2274084
rs2274084
0.010 GeneticVariation BEFREE We investigated GJB2 rs2274084 polymorphism in three types of tumors, including nasophoryngeal carcinoma (NPC), gastric cancer (GC) and lymphoma. 29103018

2018

dbSNP: rs2071286
rs2071286
0.010 GeneticVariation BEFREE The significant relationship between rs2071286 and rs9461776 MAF and the increased risk for NHL, suggests their use as non-invasive markers to categorize patients at risk of lymphoma. 29069725

2017

dbSNP: rs9461776
rs9461776
0.010 GeneticVariation BEFREE The significant relationship between rs2071286 and rs9461776 MAF and the increased risk for NHL, suggests their use as non-invasive markers to categorize patients at risk of lymphoma. 29069725

2017

dbSNP: rs397507444
rs397507444
0.050 GeneticVariation BEFREE Αnalysis according to lymphoma subtype revealed increased frequency of c. 677C > T TT genotype and T allele, as well as reduced prevalence of the c. 1298A > C C allele in the pSS non-MALT group compared to controls and patients without NHL. 28779180

2017

dbSNP: rs1217691063
rs1217691063
0.030 GeneticVariation BEFREE Αnalysis according to lymphoma subtype revealed increased frequency of c. 677C > T TT genotype and T allele, as well as reduced prevalence of the c. 1298A > C C allele in the pSS non-MALT group compared to controls and patients without NHL. 28779180

2017

dbSNP: rs1805087
rs1805087
MTR
0.030 GeneticVariation BEFREE The results in this meta-analysis suggest no association between the MS A2756G polymorphism and lymphoma risk; however, the GG homozygous and G alleles could decrease the lymphoma risk in Caucasians. 28742198

2017

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE HLA class I-restricted <i>MYD88</i> L265P-derived peptides as specific targets for lymphoma immunotherapy. 28405493

2017

dbSNP: rs1042752
rs1042752
0.010 GeneticVariation BEFREE We found that rs1042752-located in the 3'-UTR of POU2AF1, which plays a vital role in lymphomagenesis-was significantly associated with lymphoma risk in a case-control study with 793 patients and 939 controls. 28345816

2017

dbSNP: rs11540652
rs11540652
0.720 GeneticVariation BEFREE We previously showed that the HSP90 inhibitor ganetespib potently suppresses T-lymphoma initiation and progression and extends overall survival (OS) in hotspot knockin mice expressing the p53 gain-of-function mutants R175H and R248Q (mutp53) by 30-59%. 28300840

2017

dbSNP: rs28934578
rs28934578
0.010 GeneticVariation BEFREE We previously showed that the HSP90 inhibitor ganetespib potently suppresses T-lymphoma initiation and progression and extends overall survival (OS) in hotspot knockin mice expressing the p53 gain-of-function mutants R175H and R248Q (mutp53) by 30-59%. 28300840

2017

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE The MYD88 missense mutation c.794T>C, p.Leu265Pro, is found in patients with Waldenstörm's macroglobulinemia and lymphoma. 28042684

2017