Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918474
rs121918474
PROS1
0.010 GeneticVariation BEFREE We found that protein S K196E mutation was identified in 4 out of 233 patients with recurrent miscarriage and in 2 out of 114 patients with FGR and/or IUFD. 24613695

2014
dbSNP: rs1799963
rs1799963
F2
0.010 GeneticVariation BEFREE A combination of alleles G of rs1799963, A of rs6046, and G of rs1800790 (OR = 0.31) reduces the risk of FGR. 28544373

2017
dbSNP: rs1800790
rs1800790
FGB
0.010 GeneticVariation BEFREE A combination of alleles G of rs1799963, A of rs6046, and G of rs1800790 (OR = 0.31) reduces the risk of FGR. 28544373

2017
dbSNP: rs6046
rs6046
F7
0.010 GeneticVariation BEFREE Polymorphism rs6046 of the FVII gene is associated with the development of FGR. 28544373

2017
dbSNP: rs1217691063
rs1217691063
MTHFR
0.070 GeneticVariation BEFREE MTHFR C677T and A1298C were not associated with preeclampsia (OR, 1.06; 95% CI, 0.97-1.16 and OR, 1.16; 95% CI, 0.97-1.39, respectively), and C677T was not associated with placental abruption (OR, 1.03; 95% CI, 0.87-1.21), intrauterine growth retardation (OR, 1.02; 95% CI, 0.90-1.15), or congenital heart disease (OR, 1.05; 95% CI, 0.89-1.25). 30474229

2019
dbSNP: rs397507444
rs397507444
MTHFR
0.030 GeneticVariation BEFREE MTHFR C677T and A1298C were not associated with preeclampsia (OR, 1.06; 95% CI, 0.97-1.16 and OR, 1.16; 95% CI, 0.97-1.39, respectively), and C677T was not associated with placental abruption (OR, 1.03; 95% CI, 0.87-1.21), intrauterine growth retardation (OR, 1.02; 95% CI, 0.90-1.15), or congenital heart disease (OR, 1.05; 95% CI, 0.89-1.25). 30474229

2019