Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
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: 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: 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: rs867329357
rs867329357
0.010 GeneticVariation BEFREE Herein we performed a case-control study evaluating the influence of three single nucleotide polymorphisms (SNPs) in XPA, ERCC5 and MTR [rs1800975 (G-4A), rs17655 (Asp1104His) and rs1805087 (A2756G), respectively] in lymphoma risk. 23818366

2013

dbSNP: rs267601394
rs267601394
A 0.720 GeneticVariation CLINVAR Selective inhibition of EZH2 by EPZ-6438 leads to potent antitumor activity in EZH2-mutant non-Hodgkin lymphoma. 24563539

2014

dbSNP: rs267601394
rs267601394
G 0.720 GeneticVariation CLINVAR A selective inhibitor of EZH2 blocks H3K27 methylation and kills mutant lymphoma cells. 23023262

2012

dbSNP: rs267601394
rs267601394
0.720 GeneticVariation BEFREE As EZH2 mutations often coincide with other mutations in lymphoma, we combined the expression of EZH2(Y641F) by crossing these transgenic mice with Eµ-Myc transgenic mice. 24802772

2014

dbSNP: rs267601394
rs267601394
0.720 GeneticVariation BEFREE These results suggest that Ezh2(Y641F) induces lymphoma and melanoma through a vast reorganization of chromatin structure, inducing both repression and activation of polycomb-regulated loci. 27135738

2016

dbSNP: rs267601394
rs267601394
A 0.720 GeneticVariation CLINVAR A selective inhibitor of EZH2 blocks H3K27 methylation and kills mutant lymphoma cells. 23023262

2012

dbSNP: rs1057519833
rs1057519833
0.710 GeneticVariation BEFREE Herein, we identify mutation of EZH2 A677 to a glycine (A677G) among lymphoma cell lines and primary tumor specimens. 22323599

2012

dbSNP: rs1057519833
rs1057519833
C 0.710 GeneticVariation CLINVAR A selective inhibitor of EZH2 blocks H3K27 methylation and kills mutant lymphoma cells. 23023262

2012

dbSNP: rs267601395
rs267601395
G 0.700 GeneticVariation CLINVAR A selective inhibitor of EZH2 blocks H3K27 methylation and kills mutant lymphoma cells. 23023262

2012

dbSNP: rs267601395
rs267601395
T 0.700 GeneticVariation CLINVAR A selective inhibitor of EZH2 blocks H3K27 methylation and kills mutant lymphoma cells. 23023262

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: 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: 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: rs995922697
rs995922697
0.010 GeneticVariation BEFREE Data from two population-based, case-control studies of lymphoma in the UK (700 cases and 915 controls) and USA (1593 cases and 2517 controls) were pooled to analyze polymorphisms in genes involved in the oxidative stress response (SOD2 Val16Ala, CAT C-262T and GPX1 Pro197Leu). 16956821

2006

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: 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: rs9268853
rs9268853
C 0.800 GeneticVariation GWASCAT Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies. 23349640

2013

dbSNP: rs9268853
rs9268853
C 0.800 GeneticVariation GWASDB Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies. 23349640

2013

dbSNP: rs2395185
rs2395185
0.010 GeneticVariation BEFREE We replicated a strong risk association in non-Hispanic White males with rs2395185, a protective marker for lymphoma. 24707947

2015

dbSNP: rs2304240
rs2304240
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: 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