Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10261922
rs10261922 		A 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250

2013
dbSNP: rs1037351
rs1037351
DDC ; FIGNL1
C 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250

2013
dbSNP: rs1045642
rs1045642
ABCB1
0.030 GeneticVariation BEFREE MDR1 C3435T polymorphism in Mexican children with acute lymphoblastic leukemia and in healthy individuals. 19317599

2008
dbSNP: rs1045642
rs1045642
ABCB1
0.030 GeneticVariation BEFREE Analysis of single nucleotide polymorphism C3435T of the multidrug resistance gene MDR1 in acute lymphoblastic leukemia. 12851703

2003
dbSNP: rs1045642
rs1045642
ABCB1
0.030 GeneticVariation BEFREE Is the MDR1 C3435T polymorphism responsible for oral mucositis in children with acute lymphoblastic leukemia? 23244145

2012
dbSNP: rs1057519695
rs1057519695
NRAS
0.010 GeneticVariation BEFREE Early T-Cell Precursor Acute Lymphoblastic Leukemia in an Infant With an NRAS Q61R Mutation and Clinical Features of Juvenile Myelomonocytic Leukemia. 27145535

2016
dbSNP: rs1057519753
rs1057519753
JAK1
0.010 GeneticVariation BEFREE This mutation was identical to the JAK1 V658F mutation previously found in human APL and acute lymphoblastic leukemia samples. 21436584

2011
dbSNP: rs1057519773
rs1057519773
ABL1
0.010 GeneticVariation BEFREE At the first relapse, an examination of the bone marrow revealed a transformation into acute lymphoblastic leukemia and an F317L mutation in BCR-ABL1 gene, which responded preferentially to nilotinib over dasatinib. 24532437

2014
dbSNP: rs1057519834
rs1057519834
NRAS
0.010 GeneticVariation BEFREE Early T-Cell Precursor Acute Lymphoblastic Leukemia in an Infant With an NRAS Q61R Mutation and Clinical Features of Juvenile Myelomonocytic Leukemia. 27145535

2016
dbSNP: rs10740055
rs10740055
ARID5B
0.010 GeneticVariation BEFREE Furthermore, the recessive models revealed that six SNPs were risk factors for acute lymphoblastic leukemia: rs10740055, rs7089424, rs10994982, rs7896246, rs10821938, and rs7923074. 28381164

2017
dbSNP: rs10821936
rs10821936
ARID5B
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: rs10821936
rs10821936
ARID5B
C 0.810 GeneticVariation GWASCAT Family-based exome-wide association study of childhood acute lymphoblastic leukemia among Hispanics confirms role of ARID5B in susceptibility. 28817678

2017
dbSNP: rs10821936
rs10821936
ARID5B
C 0.810 GeneticVariation GWASCAT Germline genomic variants associated with childhood acute lymphoblastic leukemia. 19684603

2009
dbSNP: rs10821936
rs10821936
ARID5B
C 0.810 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250

2013
dbSNP: rs10821936
rs10821936
ARID5B
C 0.810 GeneticVariation GWASDB Germline genomic variants associated with childhood acute lymphoblastic leukemia. 19684603

2009
dbSNP: rs10821936
rs10821936
ARID5B
C 0.810 GeneticVariation GWASCAT Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia. 22076464

2012
dbSNP: rs10821936
rs10821936
ARID5B
C 0.810 GeneticVariation GWASCAT Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250

2013
dbSNP: rs10821938
rs10821938
ARID5B
A 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250

2013
dbSNP: rs10899736
rs10899736
DDC ; FIGNL1
C 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250

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

2009
dbSNP: rs11013046
rs11013046
PIP4K2A
A 0.700 GeneticVariation GWASDB Novel susceptibility variants at 10p12.31-12.2 for childhood acute lymphoblastic leukemia in ethnically diverse populations. 23512250

2013
dbSNP: rs1110701
rs1110701 		G 0.700 GeneticVariation GWASCAT Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures. 25310577

2014