Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587776632
rs587776632
GAA 0.700 CausalMutation CLINVAR

dbSNP: rs587776633
rs587776633
CT 0.700 CausalMutation CLINVAR

dbSNP: rs587776634
rs587776634
C 0.700 CausalMutation CLINVAR

dbSNP: rs587776635
rs587776635
A 0.700 CausalMutation CLINVAR

dbSNP: rs587776636
rs587776636
GA 0.700 CausalMutation CLINVAR

dbSNP: rs587776637
rs587776637
C 0.700 CausalMutation CLINVAR

dbSNP: rs854560
rs854560
0.010 GeneticVariation BEFREE The numbers of cases of particular subtypes were rather small for stable estimates, but we noted that the PON1 L55M AA allele, associated with slightly increased risk of non-Hodgkin's lymphoma (variant homozygotes OR, 1.36; 95% CI, 0.96-1.95), was most strongly associated with follicular non-Hodgkin's lymphoma and T-cell lymphoma, with ORs for variant homozygotes of 2.12 and 2.93, respectively. 16985026

2006

dbSNP: rs1695
rs1695
0.010 GeneticVariation BEFREE We studied deletions of GSTM1 and GSTT1, and the GSTP1 Ile(105)Val polymorphism in 89 patients with follicular lymphoma (FL). 17454600

2007

dbSNP: rs587781386
rs587781386
0.010 GeneticVariation BEFREE Double transversion mutations comprising of a missense mutation at codon 167 (Gln to His) in exon 5 and a nonsense mutation at codon 183 (Ser to stop codon) in exon 5 were detected in one DLBL that had apparently transformed from follicular lymphoma and in one advanced adult T-cell lymphoma (ATL). 17609875

2007

dbSNP: rs764562217
rs764562217
0.010 GeneticVariation BEFREE Double transversion mutations comprising of a missense mutation at codon 167 (Gln to His) in exon 5 and a nonsense mutation at codon 183 (Ser to stop codon) in exon 5 were detected in one DLBL that had apparently transformed from follicular lymphoma and in one advanced adult T-cell lymphoma (ATL). 17609875

2007

dbSNP: rs3020314
rs3020314
0.010 GeneticVariation BEFREE Four ESR1 SNPs were associated with follicular lymphoma (FL) in the U.S. study, with rs3020314 remaining associated with reduced risk of FL after multiple testing adjustments [odds ratio (OR) = 0.42, 95% confidence interval (CI) = 0.23-0.77) and replication in the German study (OR = 0.24, 95% CI = 0.06-0.94). 18636124

2008

dbSNP: rs172378
rs172378
0.010 GeneticVariation BEFREE Genotyping for C1qA([276A/G]) was done in 133 subjects with follicular lymphoma treated with single-agent rituximab, and correlation with clinical response was done using Cox regression analysis. 18927313

2008

dbSNP: rs372411058
rs372411058
0.010 GeneticVariation BEFREE Genotyping for C1qA([276A/G]) was done in 133 subjects with follicular lymphoma treated with single-agent rituximab, and correlation with clinical response was done using Cox regression analysis. 18927313

2008

dbSNP: rs3789068
rs3789068
0.010 GeneticVariation BEFREE Variants in BCL2L11 were strongly related to follicular lymphoma only, particularly rs3789068 (OR(AG), 1.41; 95% CI, 1.10-1.81; OR(GG), 1.65; 95% CI, 1.25-2.19; P(trend) = 0.0004). 19336552

2009

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: rs6457327
rs6457327
C 0.750 GeneticVariation GWASDB We found that rs6457327 on 6p21.33 was associated with susceptibility to follicular lymphoma (FL; N = 189 cases, 592 controls) with validation in another 456 FL cases and 2,785 controls (combined allelic P = 4.7 x 10(-11)). 19620980

2009

dbSNP: rs6457327
rs6457327
0.750 GeneticVariation BEFREE We found that rs6457327 on 6p21.33 was associated with susceptibility to follicular lymphoma (FL; N = 189 cases, 592 controls) with validation in another 456 FL cases and 2,785 controls (combined allelic P = 4.7 x 10(-11)). 19620980

2009

dbSNP: rs1308699981
rs1308699981
0.010 GeneticVariation BEFREE Here, we analyzed the FcgammaRIIIa 158 V/F, FcgammaRIIa 131 H/R, and FcgammaRIIb 232 I/T polymorphisms in a group of 188 patients with follicular lymphoma who were treated with chemotherapy without rituximab initially. 19672774

2009

dbSNP: rs1217691063
rs1217691063
0.030 GeneticVariation BEFREE We studied the association between the different genotypes of the two most common MTHFR polymorphisms, C677T and A1298C, and the risk of follicular lymphoma (FL). 19963111

2009

dbSNP: rs397507444
rs397507444
0.020 GeneticVariation BEFREE The frequency of the A1298C CC homozygous mutant genotype was significantly higher in patients with FL than in control subjects (OR = 3.51, 95% CI = 1.39-8.86, P = 0.008). 19963111

2009

dbSNP: rs2228479
rs2228479
0.010 GeneticVariation BEFREE The variant allele at V92M was associated with FL (odds ratio (OR)=1.61, 95% confidence interval (CI) 1.08-2.39) and the r:wild type genotype with DLBCL (OR=0.58, 95% CI 0.38-0.89). 20129839

2010

dbSNP: rs1883832
rs1883832
0.010 GeneticVariation BEFREE Data from earlier studies that are part of this pooling study implicate a functional polymorphism (-1C>T, rs1883832) in the TNFRSF5 gene encoding CD40 in the etiology of follicular lymphoma. 20473910

2011

dbSNP: rs10484561
rs10484561
G 0.770 GeneticVariation GWASDB We identified two variants associated with follicular lymphoma at 6p21.32 (rs10484561, combined P = 1.12 x 10(-29) and rs7755224, combined P = 2.00 x 10(-19); r(2) = 1.0), supporting the idea that major histocompatibility complex genetic variation influences follicular lymphoma susceptibility. 20639881

2010

dbSNP: rs10484561
rs10484561
0.770 GeneticVariation BEFREE We identified two variants associated with follicular lymphoma at 6p21.32 (rs10484561, combined P = 1.12 x 10(-29) and rs7755224, combined P = 2.00 x 10(-19); r(2) = 1.0), supporting the idea that major histocompatibility complex genetic variation influences follicular lymphoma susceptibility. 20639881

2010

dbSNP: rs735665
rs735665
T 0.700 GeneticVariation GWASDB Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32. 20639881

2010