Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE <b>Results</b> We found that the early pregnancy loss (EPL) rate increased as MTHFR polymorphism complexity increased and that the early EPL rate was significantly higher in patients with MTHFR C677T polymorphism compared to patients with MTHFR A1298C polymorphism (p = 0.039). 30258247

2018

dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE MTHFR C677T polymorphism and recurrent early pregnancy loss risk in north Indian population. 22138544

2012

dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE The methylenetetrahydrofolate reductase (MTHFR) gene C677T and A1298C polymorphisms are commonly associated with defects in folate dependent homocysteine metabolism and have been implicated as risk factors for recurrent embryo loss in early pregnancy. 11938441

2002

dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE Because of MTHFR's involvement with folate metabolism and evidence that maternal use of a multivitamin with folic acid in early pregnancy reduces risk for cleft lip with or without cleft palate (CLP), we hypothesized that infants homozygous for the C677T genotype would be at increased risk for CLP because of lower MTHFR enzymatic activity. 9843036

1998

dbSNP: rs397507444
rs397507444
0.020 GeneticVariation BEFREE <b>Results</b> We found that the early pregnancy loss (EPL) rate increased as MTHFR polymorphism complexity increased and that the early EPL rate was significantly higher in patients with MTHFR C677T polymorphism compared to patients with MTHFR A1298C polymorphism (p = 0.039). 30258247

2018

dbSNP: rs397507444
rs397507444
0.020 GeneticVariation BEFREE The methylenetetrahydrofolate reductase (MTHFR) gene C677T and A1298C polymorphisms are commonly associated with defects in folate dependent homocysteine metabolism and have been implicated as risk factors for recurrent embryo loss in early pregnancy. 11938441

2002

dbSNP: rs1569686
rs1569686
0.010 GeneticVariation BEFREE Considering the growing evidence on the important roles of DNA methylation in gametogenesis and early pregnancy, we investigated the potential association of DNA methyltransferase gene polymorphisms (DNMT1 rs2228611, DNMT3A rs1550117, DNMT3B rs1569686) with RSA in Slovenian reproductive couples. 28940947

2017

dbSNP: rs2228611
rs2228611
0.010 GeneticVariation BEFREE Considering the growing evidence on the important roles of DNA methylation in gametogenesis and early pregnancy, we investigated the potential association of DNA methyltransferase gene polymorphisms (DNMT1 rs2228611, DNMT3A rs1550117, DNMT3B rs1569686) with RSA in Slovenian reproductive couples. 28940947

2017

dbSNP: rs117106081
rs117106081
0.010 GeneticVariation BEFREE In conclusion, PROKR1 (I379V) and PROKR2 (V331M) variants conferred lower risk for RM and may play protective roles in early pregnancy by altering calcium signaling and facilitating cell invasiveness. 23687280

2013

dbSNP: rs1421868342
rs1421868342
0.010 GeneticVariation BEFREE In conclusion, PROKR1 (I379V) and PROKR2 (V331M) variants conferred lower risk for RM and may play protective roles in early pregnancy by altering calcium signaling and facilitating cell invasiveness. 23687280

2013

dbSNP: rs34715748
rs34715748
0.010 GeneticVariation BEFREE In conclusion, PROKR1 (I379V) and PROKR2 (V331M) variants conferred lower risk for RM and may play protective roles in early pregnancy by altering calcium signaling and facilitating cell invasiveness. 23687280

2013

dbSNP: rs1799983
rs1799983
0.010 GeneticVariation BEFREE Our results do not show any influence of the two polymorphisms, VNTR in intron 4 and Glu298Asp of the eNOS gene, on early pregnancy. 18299866

2008