Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1135401746
rs1135401746
G 0.700 GeneticVariation CLINVAR

dbSNP: rs121909646
rs121909646
0.700 GeneticVariation UNIPROT

dbSNP: rs121913232
rs121913232
0.700 GeneticVariation UNIPROT

dbSNP: rs121913487
rs121913487
0.700 GeneticVariation UNIPROT

dbSNP: rs121913488
rs121913488
0.700 GeneticVariation UNIPROT

dbSNP: rs1478147351
rs1478147351
0.700 GeneticVariation UNIPROT

dbSNP: rs186148199
rs186148199
0.700 GeneticVariation UNIPROT

dbSNP: rs188887061
rs188887061
0.700 GeneticVariation UNIPROT

dbSNP: rs398123063
rs398123063
0.700 GeneticVariation UNIPROT

dbSNP: rs10821936
rs10821936
0.810 GeneticVariation BEFREE <i>ARID5B</i> rs10821936 and rs10994982 gene polymorphisms and acute lymphoblastic leukemia: relation to disease susceptibility and outcome. 31424309

2019

dbSNP: rs10994982
rs10994982
0.710 GeneticVariation BEFREE <i>ARID5B</i> rs10821936 and rs10994982 gene polymorphisms and acute lymphoblastic leukemia: relation to disease susceptibility and outcome. 31424309

2019

dbSNP: rs4553808
rs4553808
0.010 GeneticVariation BEFREE 153 donors and 153 children with acute lymphoblastic leukemia, acute myeloid leukemia or juvenile myelomonocytic leukemia who had undergone allogeneic HSCT were genotyped of CTLA-4 gene for rs3087243 (CT60G>A), rs231775 (+ 49 A>G) and rs4553808 using TaqMan real-time polymerase chain reaction. 29335768

2018

dbSNP: rs231775
rs231775
0.010 GeneticVariation BEFREE 153 donors and 153 children with acute lymphoblastic leukemia, acute myeloid leukemia or juvenile myelomonocytic leukemia who had undergone allogeneic HSCT were genotyped of CTLA-4 gene for rs3087243 (CT60G>A), rs231775 (+ 49 A>G) and rs4553808 using TaqMan real-time polymerase chain reaction. 29335768

2018

dbSNP: rs766639320
rs766639320
0.010 GeneticVariation BEFREE 153 donors and 153 children with acute lymphoblastic leukemia, acute myeloid leukemia or juvenile myelomonocytic leukemia who had undergone allogeneic HSCT were genotyped of CTLA-4 gene for rs3087243 (CT60G>A), rs231775 (+ 49 A>G) and rs4553808 using TaqMan real-time polymerase chain reaction. 29335768

2018

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE A common C to T transition (C677T) in the MTHFR gene is reported to reduce the risk for colorectal cancer and acute lymphocytic leukemia in homozygotes (TTs). 11408344

2001

dbSNP: rs3824662
rs3824662
A 0.800 GeneticVariation GWASCAT A genome-wide association study of susceptibility to acute lymphoblastic leukemia in adolescents and young adults. 25468567

2015

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE A meta-analysis of MTHFR C677T and A1298C polymorphisms and risk of acute lymphoblastic leukemia in children. 21495160

2012

dbSNP: rs397507444
rs397507444
0.070 GeneticVariation BEFREE A meta-analysis of MTHFR C677T and A1298C polymorphisms and risk of acute lymphoblastic leukemia in children. 21495160

2012

dbSNP: rs2274407
rs2274407
0.010 GeneticVariation BEFREE ABCC4 functional SNP in the 3' splice acceptor site of exon 8 (G912T) is associated with unfavorable clinical outcome in children with acute lymphoblastic leukemia. 28550450

2017

dbSNP: rs1045642
rs1045642
0.030 GeneticVariation BEFREE Analysis of single nucleotide polymorphism C3435T of the multidrug resistance gene MDR1 in acute lymphoblastic leukemia. 12851703

2003

dbSNP: rs1217691063
rs1217691063
0.100 GeneticVariation BEFREE Association Between the 5,10-MTHFR 677C>T and RFC1 80G>A Polymorphisms and Acute Lymphoblastic Leukemia. 31499477

2019

dbSNP: rs12786200
rs12786200
0.700 GeneticVariation GWASCAT Association of an inherited genetic variant with vincristine-related peripheral neuropathy in children with acute lymphoblastic leukemia. 25710658

2015

dbSNP: rs17032980
rs17032980
0.700 GeneticVariation GWASCAT Association of an inherited genetic variant with vincristine-related peripheral neuropathy in children with acute lymphoblastic leukemia. 25710658

2015

dbSNP: rs4463516
rs4463516
0.700 GeneticVariation GWASCAT Association of an inherited genetic variant with vincristine-related peripheral neuropathy in children with acute lymphoblastic leukemia. 25710658

2015

dbSNP: rs7818688
rs7818688
0.700 GeneticVariation GWASCAT Association of an inherited genetic variant with vincristine-related peripheral neuropathy in children with acute lymphoblastic leukemia. 25710658

2015