rs1188383936, F2

N. diseases: 102
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Fetal Growth Retardation
CUI: C0015934
Disease: Fetal Growth Retardation
0.030 GeneticVariation BEFREE The following number of related studies were found: studies evaluating relationships between factor V Leiden mutation and IUGR, 12 case-control and four cohort; between PT mutation and IUGR, 11 case-control and 0 cohort; and between MTHFR C677T homozygosity and IUGR, 10 case-control and two cohort. 19461414 2009
Fetal Growth Retardation
CUI: C0015934
Disease: Fetal Growth Retardation
0.030 GeneticVariation BEFREE No association was found in this study between intrauterine growth restriction with abnormal umbilical blood flow and thrombophilic polymorphisms or methylenetetrahydrofolate reductase C677T. 15075078 2004
Fetal Growth Retardation
CUI: C0015934
Disease: Fetal Growth Retardation
0.030 GeneticVariation BEFREE Newborns who were homozygous for the MTHFR C677T variant had a decreased risk of intrauterine growth restriction (odds ratio after adjustment for mother's genotype and other confounders, 0.52 [95 percent confidence interval, 0.29 to 0.94]). 12097536 2002