Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1063045
rs1063045
NBN
CUI: C0025202
Disease: melanoma
melanoma 		0.010 GeneticVariation BEFREE No significant associations between single nucleotide polymorphisms (rs9995, rs867185 and rs1063045) or referring calculated haplotypes and melanoma risk were identified. 17496786

2007