Gene: NBN ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4683
Gene Symbol: NBN
NBN 		0.630 GeneticVariation disease BEFREE Functional polymorphisms in the NBS1 gene and acute lymphoblastic leukemia susceptibility in a Chinese population. 21166880 2011
Entrez Id: 4683
Gene Symbol: NBN
NBN 		0.630 GeneticVariation disease LHGDN Carrier frequency of mutation 657del5 in the NBS1 gene in a population of Polish pediatric patients with sporadic lymphoid malignancies. 16152606 2006
Entrez Id: 4683
Gene Symbol: NBN
NBN 		0.630 Biomarker disease GENOMICS_ENGLAND 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 		0.630 GeneticVariation disease 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 		0.630 Biomarker disease GENOMICS_ENGLAND Mutations in the Nijmegen Breakage Syndrome gene (NBS1) in childhood acute lymphoblastic leukemia (ALL). 11325820 2001
Entrez Id: 4683
Gene Symbol: NBN
NBN 		0.630 Biomarker disease CTD_human
Entrez Id: 4683
Gene Symbol: NBN
NBN 		0.630 Biomarker disease HPO