Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1448674651
rs1448674651
TYMS ; ENOSF1
0.030 GeneticVariation BEFREE Children with ALL (n = 96) were screened for GCPII C1561T, RFC1 G80A, cSHMT C1420T, TYMS 5´-UTR 2R3R, TYMS 3´-UTR ins6/del6, MTHFR C677T, MTR A2756G polymorphisms using PCR-RFLP and PCR-amplified fragment length polymorphism techniques. 22838948

2012
dbSNP: rs1448674651
rs1448674651
TYMS ; ENOSF1
0.030 GeneticVariation BEFREE SLC19A1 80G > A emerged as the predominant polymorphism associated with risk of ALL. 20824655

2011
dbSNP: rs1448674651
rs1448674651
TYMS ; ENOSF1
0.030 GeneticVariation BEFREE For the first time, we associate the RFC1 80G>A and NNMT IVS -151C>T variants to an increased ALL susceptibility. 19020309

2009