Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1051266
rs1051266
SLC19A1
0.060 GeneticVariation BEFREE The BHMT gene rs3733890, RFC1 gene rs1051266 and MTR gene rs1805087 were associated with the occurrence of NTDs in Han population of Northern China. 28770393

2018
dbSNP: rs1051266
rs1051266
SLC19A1
0.060 GeneticVariation BEFREE In SLC19A1, c.80A>G (rs1051266) was not associated with our MM cohort; we did observe a variant allele G frequency of 61.7%, higher than previously reported in other NTD populations. 28948692

2017
dbSNP: rs1051266
rs1051266
SLC19A1
0.060 GeneticVariation BEFREE The aim of this study was to investigate whether the risk for NTDs was influenced by the interactions between the SLC19A1 (rs1051266) variant and maternal first trimester fever. 24917213

2015
dbSNP: rs1051266
rs1051266
SLC19A1
0.060 GeneticVariation BEFREE Our meta-analysis strongly suggested a significant association of the variant MTHFR C677T and a suggestive association of RFC-1 A80G with increased risk of NTDs. 23593147

2013
dbSNP: rs1051266
rs1051266
SLC19A1
0.060 GeneticVariation BEFREE The RFC1 is likely to be an important candidate gene in folate transportation and RFC1 GG genotype (A80G) may be associated with an increased risk for NTDs in this Chinese population. 19105199

2009
dbSNP: rs1051266
rs1051266
SLC19A1
0.060 GeneticVariation BEFREE Altogether, our findings support the hypothesis that RFC-1 A80G variant may contribute to NTD susceptibility in the Italian population. 12673279

2003