Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs75873440
rs75873440
RET
0.010 GeneticVariation BEFREE Familial MTC with <i>RET</i> exon 8 Gly533Cys mutation: origin and prevalence of second malignancy. 28951487

2017
dbSNP: rs397507444
rs397507444
MTHFR
0.010 GeneticVariation BEFREE The relative risk for second malignancy was not significantly increased in ALL patients having at least one polymorphic C667T [odds ratio (OR) 1.51; 95% confidence interval (CI) 0.43-5.31] or one polymorphic A1298C allele (OR 1; 95% CI 0.29?-?3.46). 16019535

2005