Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4683
Gene Symbol: NBN
NBN
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		0.140 GeneticVariation BEFREE NBN and XRCC3 genetic variants in childhood acute lymphoblastic leukaemia. 25176580

2014
Entrez Id: 4683
Gene Symbol: NBN
NBN
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		0.140 GeneticVariation BEFREE These findings suggest that E185Q polymorphism in NBS1 may be a genetic modifier for developing ALL. 21166880

2011
Entrez Id: 4683
Gene Symbol: NBN
NBN
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		0.140 GeneticVariation BEFREE The NBS1 mutation 657del5 on one allele was found in 3 of 270 patients with ALL and 2 of 212 children and adolescents with NHL; no carrier was found among 63 patients with Hodgkin lymphoma (HL). 16152606

2006
Entrez Id: 4683
Gene Symbol: NBN
NBN
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		0.140 GeneticVariation BEFREE Four children with acute lymphoblastic leukemia have been reported to be heterozygous for a germline and/or somatic missense mutation in NBS1, leading to the I171V substitution. 15338273

2004
Entrez Id: 4683
Gene Symbol: NBN
NBN
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		0.140 CausalMutation CLINVAR

Entrez Id: 4683
Gene Symbol: NBN
NBN
CUI: C0023449
Disease: Acute lymphocytic leukemia
Acute lymphocytic leukemia 		0.140 GeneticVariation CLINVAR