Gene: NBN ×
Source: BEFREE ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1805794
rs1805794
NBN
0.010 GeneticVariation BEFREE These findings suggest that E185Q polymorphism in NBS1 may be a genetic modifier for developing ALL. 21166880

2011
dbSNP: rs2735383
rs2735383
OSGIN2 ; NBN
0.010 GeneticVariation BEFREE Besides, there is no report about the association between NBS1 3'UTR variant rs2735383 and ALL risk. 21166880

2011
dbSNP: rs34767364
rs34767364
NBN
0.010 GeneticVariation BEFREE In addition, the substitution 643C>T (R215W) has also been found in excess among children with acute lymphoblastic leukemia (ALL). 16152606

2006
dbSNP: rs61754966
rs61754966
NBN
0.010 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