Gene: SLC19A1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1051296
rs1051296
SLC19A1
0.010 GeneticVariation BEFREE Genotyping for SLC19A1 rs1051296 G>T in 131 children with ALL was performed using the Sequenom MassArray system. 24927955

2014
dbSNP: rs1051266
rs1051266
SLC19A1
0.010 GeneticVariation BEFREE There was evidence that the minor alleles of NOS3 rs3918186 (OR = 2.16; 95% CI: 1.51-3.15) and SLC19A1 rs1051266 (OR = 2.07; 95% CI: 1.25-3.46) were positively associated with childhood ALL. 24367687

2013
dbSNP: rs775144154
rs775144154
SLC19A1
0.010 GeneticVariation BEFREE The association of reduced folate carrier 80G>A polymorphism to outcome in childhood acute lymphoblastic leukemia interacts with chromosome 21 copy number. 20335220

2010
dbSNP: rs138047632
rs138047632
SLC19A1 ; LOC107987304
0.010 GeneticVariation BEFREE A missense mutation affecting the 11th transmembrane domain of RFC (c.1250T>C; p.I417T) was found in one case of ALL at diagnosis. 18028428

2008
dbSNP: rs569954362
rs569954362
SLC19A1
0.010 GeneticVariation BEFREE A high-abundance C/T696 polymorphism was detected with nearly identical frequencies for both alleles, and a heterozygous C/A1242 sequence variant was identified in two ALL specimens. 11705857

2001
dbSNP: rs57725551
rs57725551
SLC19A1 ; LOC107987304
0.010 GeneticVariation BEFREE A high-abundance C/T696 polymorphism was detected with nearly identical frequencies for both alleles, and a heterozygous C/A1242 sequence variant was identified in two ALL specimens. 11705857

2001