Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11540652
rs11540652
T 0.720 GeneticVariation CLINVAR

dbSNP: rs121434629
rs121434629
A 0.700 GeneticVariation CLINVAR

dbSNP: rs121918459
rs121918459
G 0.700 CausalMutation CLINVAR

dbSNP: rs267608150
rs267608150
CTTCACACACA 0.700 CausalMutation CLINVAR

dbSNP: rs555607708
rs555607708
A 0.700 CausalMutation CLINVAR

dbSNP: rs63750250
rs63750250
AT 0.700 CausalMutation CLINVAR

dbSNP: rs869312777
rs869312777
G 0.700 GeneticVariation CLINVAR

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: rs1217691063
rs1217691063
0.030 GeneticVariation BEFREE C677T and A1298C methylenetetrahydrofolate reductase (MTHFR) polymorphisms have been suggested to affect susceptibility to malignant lymphoma, possibly by altering DNA methylation. 14535593

2004

dbSNP: rs773919809
rs773919809
0.010 GeneticVariation BEFREE C677T and A1298C methylenetetrahydrofolate reductase (MTHFR) polymorphisms have been suggested to affect susceptibility to malignant lymphoma, possibly by altering DNA methylation. 14535593

2004

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: rs2230926
rs2230926
0.040 GeneticVariation BEFREE A germline and coding polymorphism (rs2230926) of TNFAIP3 (A20), a central gatekeeper of nuclear factor-kappa B (NF-kB) activation, was recently found associated with primary Sjögren's syndrome (pSS)-associated lymphoma in a French cohort.We aimed to replicate this association. 26338037

2016

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

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: rs707824
rs707824
0.810 GeneticVariation BEFREE A SNP in a novel non-HLA region on 6p23 (rs707824, P(NHL) = 5.72×10(-7)) was suggestive of an association conferring susceptibility to lymphoma. 23349640

2013

dbSNP: rs707824
rs707824
T 0.810 GeneticVariation GWASCAT A SNP in a novel non-HLA region on 6p23 (rs707824, P(NHL) = 5.72×10(-7)) was suggestive of an association conferring susceptibility to lymphoma. 23349640

2013

dbSNP: rs707824
rs707824
T 0.810 GeneticVariation GWASDB A SNP in a novel non-HLA region on 6p23 (rs707824, P(NHL) = 5.72×10(-7)) was suggestive of an association conferring susceptibility to lymphoma. 23349640

2013

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: 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: rs8177400
rs8177400
0.010 GeneticVariation BEFREE Although rs8177400 did not modify lymphoma risk in general, its frequency of heterozygosity was accurately determined to 0.97%. 20164415

2010

dbSNP: rs61754966
rs61754966
NBN
0.010 GeneticVariation BEFREE Among these, an association with cancer was found most frequently for 657del5 (in leukemia/lymphoma and breast cancer) and I171V (in leukemia, breast, head and neck and colorectal cancers); however, other studies gave contradictory results. 18606567

2008

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