Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: rs10494879
rs10494879
0.010 GeneticVariation BEFREE Five hundred patients with aggressive NHL treated with CHOP/CHOEP were analyzed for IL-10 gene polymorphisms, including distal loci -7400InDel, -6752AT (rs6676671), and -6208CG (rs10494879) in comparison with proximal loci -3538AT (rs1800890), -1087AG (rs1800896), and -597AC (rs1800872) according to the incidence and outcome of the lymphoma. 18559596

2008

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: rs1131691014
rs1131691014
0.010 GeneticVariation BEFREE Through searching PubMed databases (or hand searching) up to April 2012 using the following MeSH terms and keywords: "p53", "codon 72" "polymorphism" and "leukemia", or "lymphoma", or "myeloma", thirteen were identified as eligible articles in this meta-analysis for p53 Arg72Pro polymorphism (2,731 cases and 7, 356 controls), including nine studies on leukemia (1,266 cases and 4, 474 controls), three studies on lymphoma (1,359 cases and 2,652 controls), and one study on myeloma. 23029260

2012

dbSNP: rs11466782
rs11466782
0.010 GeneticVariation BEFREE The ADAM19 rs11466782 SNP was associated with an increased risk of lymphoma (OR, 1.73; 95% CI, 1.28-2.35; Padditive=0.0004), and the ICAM3 rs2304240 (OR, 0.67; 95% CI, 0.52-0.86; Padditive=0.002) and the PTGDR rs708486 SNPs (OR, 0.75; 95% CI, 0.63-0.90; Padditive=0.002) were associated with reduced risk of lymphoma. 21239057

2011

dbSNP: rs11547328
rs11547328
0.010 GeneticVariation BEFREE We propose that similarly to typical human MCL and its blastoid or cyclin-D1 variants that correspond to the same genetic entity, MCL-like lymphomas of c-myc-3'RR/ p53+/- mice and c-myc-3'RR/Cdk4(R24C) mice represent a spectrum of the same entity. 22592113

2012

dbSNP: rs121913105
rs121913105
0.010 GeneticVariation BEFREE Constitutive phosphorylation of c-Cbl by the K650M mutant appeared to be related to the intracellular retention of the receptor. 17509076

2007

dbSNP: rs121913237
rs121913237
0.010 GeneticVariation BEFREE Using a bone marrow transplant model, we previously showed that ∼ 95% of animals receiving Nras G12D/+ bone marrow cells develop chronic myelomonocytic leukemia (CMML), while ∼ 8% of recipients develop acute T-cell lymphoblastic leukemia/lymphoma [TALL] (TALL-het). 21586752

2011

dbSNP: rs121913482
rs121913482
0.010 GeneticVariation BEFREE Internalization of the R248C and Y373C mutant receptors, which form stable disulfide-bonded dimers at the cell surface was less efficient than the wild-type, whereas ubiquitylation was markedly increased but apparently independent of the E3 ubiquitin-ligase casitas B-lineage lymphoma (c-Cbl). 17509076

2007

dbSNP: rs121913485
rs121913485
0.010 GeneticVariation BEFREE Internalization of the R248C and Y373C mutant receptors, which form stable disulfide-bonded dimers at the cell surface was less efficient than the wild-type, whereas ubiquitylation was markedly increased but apparently independent of the E3 ubiquitin-ligase casitas B-lineage lymphoma (c-Cbl). 17509076

2007

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: rs121913529
rs121913529
0.010 GeneticVariation BEFREE MYC-, K-ras(G12D)- or MYC/K-ras(G12D</span>)-induced lymphomas exhibited sustained regression upon the inactivation of either or both oncogenes. 18461184

2008

dbSNP: rs1257715362
rs1257715362
0.010 GeneticVariation BEFREE PCR-SSCP and direct DNA sequencing of exons 2 to 14 of p73 revealed a missense mutation in one primary lymphoma: a G-to-A transition, with Glu291Lys change. 11461077

2001

dbSNP: rs13181
rs13181
0.010 GeneticVariation BEFREE To investigate the relationship between DNA repair and NHL we analysed polymorphisms in XPD (R156R, D312N, K751Q) using DNA collected in a UK population-based case-control study of lymphoma. 19736055

2009

dbSNP: rs1346044
rs1346044
WRN
0.010 GeneticVariation BEFREE WRN Cys1367Arg was associated with decreased risk of NHL overall (OR: 0.71; 95% CI: 0.56-0.91; P=0.007) and DLBCL (OR: 0.66; 95% CI: 0.45-0.95; P=0.024), as well as follicular and marginal zone lymphomas. 16738949

2006

dbSNP: rs1351687973
rs1351687973
0.010 GeneticVariation BEFREE PCR-SSCP and direct DNA sequencing of exons 2 to 14 of p73 revealed a missense mutation in one primary lymphoma: a G-to-A transition, with Glu291Lys change. 11461077

2001

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: 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: rs1555525126
rs1555525126
0.010 GeneticVariation BEFREE PCR-SSCP and direct DNA sequencing of exons 2 to 14 of p73 revealed a missense mutation in one primary lymphoma: a G-to-A transition, with Glu291Lys change. 11461077

2001

dbSNP: rs1695
rs1695
0.010 GeneticVariation BEFREE Pooled results showed that the GSTT1 null polymorphism might increase the risk of lymphoma (odds ratio [OR] 2.26, 95% confidence interval [CI] 1.20, 4.24; p = 0.01; random-effects model), whereas the impact of GSTM1 and GSTP1 Ile105Val polymorphisms was not significant. 22734843

2013

dbSNP: rs17655
rs17655
0.010 GeneticVariation BEFREE Our results suggest that the rs1800975, rs17655 and rs1805087 SNPs in DNA repair and synthesis of genes do not seem to play a major role in lymphoma susceptibility. 23818366

2013

dbSNP: rs1799793
rs1799793
0.010 GeneticVariation BEFREE To investigate the relationship between DNA repair and NHL we analysed polymorphisms in XPD (R156R, D312N, K751Q) using DNA collected in a UK population-based case-control study of lymphoma. 19736055

2009

dbSNP: rs1800871
rs1800871
0.010 GeneticVariation BEFREE Carriage of at least one copy of the T allele for the IL10 rs1800871</span> (as compared to no copies) was associated with decreased AIDS-NHL risk specific to lymphomas arising from the CNS (CC vs. CT/TT: OR = 0.3; 95% CI 0.1, 0.7) but not systemically (CC vs. CT/TT: OR = 1.0; 95% CI 0.5, 1.9) (Pheterogeneity = 0.03). 20299965

2010

dbSNP: rs1800890
rs1800890
0.010 GeneticVariation BEFREE Five hundred patients with aggressive NHL treated with CHOP/CHOEP were analyzed for IL-10 gene polymorphisms, including distal loci -7400InDel, -6752AT (rs6676671), and -6208CG (rs10494879) in comparison with proximal loci -3538AT (rs1800890), -1087AG (rs1800896), and -597AC (rs1800872) according to the incidence and outcome of the lymphoma. 18559596

2008

dbSNP: rs1800975
rs1800975
XPA
0.010 GeneticVariation BEFREE Our results suggest that the rs1800975, rs17655 and rs1805087 SNPs in DNA repair and synthesis of genes do not seem to play a major role in lymphoma susceptibility. 23818366

2013