Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2621416
rs2621416
G 0.800 GeneticVariation GWASDB Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies. 23349640

2013

dbSNP: rs2621416
rs2621416
G 0.800 GeneticVariation GWASCAT Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies. 23349640

2013

dbSNP: rs2647045
rs2647045
0.800 GeneticVariation GWASDB Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies. 23349640

2013

dbSNP: rs2647045
rs2647045
0.800 GeneticVariation GWASCAT Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies. 23349640

2013

dbSNP: rs4530903
rs4530903
T 0.800 GeneticVariation GWASDB Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies. 23349640

2013

dbSNP: rs4530903
rs4530903
T 0.800 GeneticVariation GWASCAT Susceptibility loci associated with specific and shared subtypes of lymphoid malignancies. 23349640

2013

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: 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: 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: rs113488022
rs113488022
0.030 GeneticVariation BEFREE These cases illustrate the expanding spectrum of BRAF V600E-positive histiocytic and dendritic cell tumors and suggest that attention should be paid to lymphomas for possible coincident presentation of these disorders. 25787243

2015

dbSNP: rs113488022
rs113488022
0.030 GeneticVariation BEFREE The presence of the BRAF c.1799T>A V600E mutation was recently described in cases of hairy cell leukemia (HCL) but not in other common lymphomas. 23161722

2012

dbSNP: rs113488022
rs113488022
0.030 GeneticVariation BEFREE The BRAF-V600E mutation defines genetically hairy cell leukemia among B-cell leukemias and lymphomas. 23349307

2013

dbSNP: rs121913377
rs121913377
0.030 GeneticVariation BEFREE These cases illustrate the expanding spectrum of BRAF V600E-positive histiocytic and dendritic cell tumors and suggest that attention should be paid to lymphomas for possible coincident presentation of these disorders. 25787243

2015

dbSNP: rs121913377
rs121913377
0.030 GeneticVariation BEFREE The presence of the BRAF c.1799T>A V600E mutation was recently described in cases of hairy cell leukemia (HCL) but not in other common lymphomas. 23161722

2012

dbSNP: rs121913377
rs121913377
0.030 GeneticVariation BEFREE The BRAF-V600E mutation defines genetically hairy cell leukemia among B-cell leukemias and lymphomas. 23349307

2013

dbSNP: rs1883832
rs1883832
0.010 GeneticVariation BEFREE We hypothesized that single nucleotide polymorphisms (SNPs) in TNFRSF5 and TNFSF5 encoding the CD40 and CD154 proteins, respectively, influence lymphoma risk, particularly a functional TNFRSF5 SNP (-1C>T, rs1883832) associated with reduced B-cell CD40 expression. 18287517

2008

dbSNP: rs2466571
rs2466571
0.010 GeneticVariation BEFREE In line with a previous study, rs2466571 in CD46 (HR = 0.73, 95% CI 0.58-0.91, p = 0.006) showed nominal association with lymphoma progression, as did two highly linked SNPs in IL8 (rs4073 HR = 0.78, 95% CI 0.62-0.97, p = 0.02; rs2227307 HR = 0.75, 95% CI 0.60-0.94, p = 0.01) previously associated with overall survival. 25294155

2014

dbSNP: rs751837
rs751837
0.010 GeneticVariation BEFREE By following two-stage GWAS approach and an independent replication study, we identified disease susceptibility locus within intron 3 of the CDC42BPB gene on 14q32 (rs751837; P=3.30 × 10(-7) and odds ratio (OR) of 3.5), a region of frequent chromosomal translocations in lymphoma, and variant on 13q12 (rs7097; P=6.57 × 10(-6) and OR of 1.43) which harbors the notch signaling mediator, LNX2 gene. 21471979

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: rs10190751
rs10190751
0.010 GeneticVariation BEFREE A comparison of 183 patients with follicular lymphoma and 233 population controls revealed an increased lymphoma risk associated with the rs10190751 A genotype causing c-FLIP(R) expression. 19439735

2009

dbSNP: rs74790047
rs74790047
0.010 GeneticVariation BEFREE For individual cancer types, p.D140E was associated with lung cancer (adjusted OR, 3.99; 95% CI, 2.07-7.67; P < 0.001), malignant lymphoma (adjusted OR, 3.24; 95% CI, 1.43-7.33; P = 0.005), and rectum cancer (adjusted OR, 6.23; 95% CI, 2.31-16.8; P < 0.001). 25407497

2015

dbSNP: rs555607708
rs555607708
A 0.700 CausalMutation CLINVAR

dbSNP: rs2227307
rs2227307
0.010 GeneticVariation BEFREE In line with a previous study, rs2466571 in CD46 (HR = 0.73, 95% CI 0.58-0.91, p = 0.006) showed nominal association with lymphoma progression, as did two highly linked SNPs in IL8 (rs4073 HR = 0.78, 95% CI 0.62-0.97, p = 0.02; rs2227307 HR = 0.75, 95% CI 0.60-0.94, p = 0.01) previously associated with overall survival. 25294155

2014

dbSNP: rs4073
rs4073
0.010 GeneticVariation BEFREE In line with a previous study, rs2466571 in CD46 (HR = 0.73, 95% CI 0.58-0.91, p = 0.006) showed nominal association with lymphoma progression, as did two highly linked SNPs in IL8 (rs4073 HR = 0.78, 95% CI 0.62-0.97, p = 0.02; rs2227307 HR = 0.75, 95% CI 0.60-0.94, p = 0.01) previously associated with overall survival. 25294155

2014

dbSNP: rs1802710
rs1802710
0.010 GeneticVariation BEFREE Analysis of 47 brain tumors and 55 lymphomas found that 23 and 29 of them were heterozygous for rs1802710, respectively. 15010842

2004