Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1476413
rs1476413
0.020 GeneticVariation BEFREE This study aims to examine whether the presence of polymorphisms in TNF-α (rs361525 and rs1799724) and MTHFR (rs1476413 and rs9651118) genes is associated with the pathogenesis of cerebral palsy (CP). 26646537

2016

dbSNP: rs1476413
rs1476413
0.020 GeneticVariation BEFREE Subgroup analysis found statistically significant difference in allele and genotype frequencies between cases with both CP and MR (CP + MR) compared with both CP-only cases and controls at rs4846049, rs1476413 and rs1801131. 20962791

2011

dbSNP: rs9651118
rs9651118
0.010 GeneticVariation BEFREE Also, a significant increase in the risk of CP was observed to be associated with the interactions of TNF-α rs1799724 and MTHFR rs9651118 (OR 2.75, 95 % CI 1.23-6.13). 26646537

2016

dbSNP: rs1801131
rs1801131
0.010 GeneticVariation BEFREE Subgroup analysis found statistically significant difference in allele and genotype frequencies between cases with both CP and MR (CP + MR) compared with both CP-only cases and controls at rs4846049, rs1476413 and rs1801131. 20962791

2011

dbSNP: rs4846049
rs4846049
0.010 GeneticVariation BEFREE Subgroup analysis found statistically significant difference in allele and genotype frequencies between cases with both CP and MR (CP + MR) compared with both CP-only cases and controls at rs4846049, rs1476413 and rs1801131. 20962791

2011

dbSNP: rs1217691063
rs1217691063
0.010 GeneticVariation BEFREE MTHFR C677T approximately doubles the risk of CP in preterm infants. 16202738

2005