Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2191566
rs2191566
ZNF230
G 0.800 GeneticVariation GWASDB Germline genomic variants associated with childhood acute lymphoblastic leukemia. 19684603

2009
dbSNP: rs2191566
rs2191566
ZNF230
G 0.800 GeneticVariation GWASCAT Germline genomic variants associated with childhood acute lymphoblastic leukemia. 19684603

2009
dbSNP: rs2239633
rs2239633
CEBPE
G 0.800 GeneticVariation GWASDB Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. 19684604

2009
dbSNP: rs2239633
rs2239633
CEBPE
G 0.800 GeneticVariation GWASCAT Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. 19684604

2009
dbSNP: rs7089424
rs7089424
ARID5B
C 0.800 GeneticVariation GWASCAT Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. 19684604

2009
dbSNP: rs7089424
rs7089424
ARID5B
C 0.800 GeneticVariation GWASDB Loci on 7p12.2, 10q21.2 and 14q11.2 are associated with risk of childhood acute lymphoblastic leukemia. 19684604

2009
dbSNP: rs10994982
rs10994982
ARID5B
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: rs7896246
rs7896246
ARID5B
0.710 GeneticVariation BEFREE Under the dominant model, SNPs rs7073837, rs10821936, rs7896246, and rs6479778 in males only showed striking association with acute lymphoblastic leukemia. 28381164

2017
dbSNP: rs10994982
rs10994982
ARID5B
A 0.710 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250

2013
dbSNP: rs7896246
rs7896246
ARID5B
A 0.710 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250

2013
dbSNP: rs10994982
rs10994982
ARID5B
0.710 GeneticVariation GWASDB Germline genomic variants associated with childhood acute lymphoblastic leukemia. 19684603

2009
dbSNP: rs60086424
rs60086424
LOC730100
T 0.700 GeneticVariation GWASCAT Genetic predisposition to PEG-asparaginase hypersensitivity in children treated according to NOPHO ALL2008. 30450575

2019
dbSNP: rs60218192
rs60218192
HS3ST4
A 0.700 GeneticVariation GWASCAT Genetic predisposition to PEG-asparaginase hypersensitivity in children treated according to NOPHO ALL2008. 30450575

2019
dbSNP: rs73062673
rs73062673
CNOT3 ; LOC102724273
C 0.700 GeneticVariation GWASCAT Genetic predisposition to PEG-asparaginase hypersensitivity in children treated according to NOPHO ALL2008. 30450575

2019
dbSNP: rs73195662
rs73195662
CDHR3
G 0.700 GeneticVariation GWASCAT Genetic predisposition to PEG-asparaginase hypersensitivity in children treated according to NOPHO ALL2008. 30450575

2019
dbSNP: rs10949482
rs10949482
NHLRC1
T 0.700 GeneticVariation GWASCAT NT5C2 germline variants alter thiopurine metabolism and are associated with acquired NT5C2 relapse mutations in childhood acute lymphoblastic leukaemia. 30201983

2018
dbSNP: rs2069426
rs2069426
CDKN2B ; CDKN2B-AS1
A 0.700 GeneticVariation GWASCAT GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21. 29348612

2018
dbSNP: rs2290400
rs2290400
GSDMB
T 0.700 GeneticVariation GWASCAT GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21. 29348612

2018
dbSNP: rs2390536
rs2390536
SP4
A 0.700 GeneticVariation GWASCAT GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21. 29348612

2018
dbSNP: rs2622849
rs2622849
COL11A1
T 0.700 GeneticVariation GWASCAT Bone mineral density in children with acute lymphoblastic leukemia. 29266176

2018
dbSNP: rs4617118
rs4617118
CCDC26
G 0.700 GeneticVariation GWASCAT GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21. 29348612

2018
dbSNP: rs4748813
rs4748813
PIP4K2A
T 0.700 GeneticVariation GWASCAT GWAS in childhood acute lymphoblastic leukemia reveals novel genetic associations at chromosomes 17q12 and 8q24.21. 29348612

2018
dbSNP: rs79050301
rs79050301
TPMT
C 0.700 GeneticVariation GWASCAT NT5C2 germline variants alter thiopurine metabolism and are associated with acquired NT5C2 relapse mutations in childhood acute lymphoblastic leukaemia. 30201983

2018
dbSNP: rs1142345
rs1142345
TPMT
0.700 GeneticVariation GWASCAT Genomewide Approach Validates Thiopurine Methyltransferase Activity Is a Monogenic Pharmacogenomic Trait. 27564568

2017
dbSNP: rs12748152
rs12748152 		C 0.700 GeneticVariation GWASCAT Genome-Wide Study Links PNPLA3 Variant With Elevated Hepatic Transaminase After Acute Lymphoblastic Leukemia Therapy. 28090653

2017