Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs34767364
rs34767364
NBN
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
Childhood Acute Lymphoblastic Leukemia 		0.020 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: rs34767364
rs34767364
NBN
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
Childhood Acute Lymphoblastic Leukemia 		0.020 GeneticVariation BEFREE The R215W mutation was observed in one ALL but also in a population-based study and probably represents a rare sequence variant. 11325820

2001