rs1801394, FASTKD3;MTRR

N. diseases: 101
Disease: Congenital Heart Defects ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Congenital Heart Defects
CUI: C0018798
Disease: Congenital Heart Defects
0.040 GeneticVariation BEFREE Parental Genetic Variants, MTHFR 677C>T and MTRR 66A>G, Associated Differently with Fetal Congenital Heart Defect. 28758112 2017
Congenital Heart Defects
CUI: C0018798
Disease: Congenital Heart Defects
0.040 GeneticVariation BEFREE Association between methionine synthase reductase A66G polymorphism and the risk of congenital heart defects: evidence from eight case-control studies. 24913415 2014
Congenital Heart Defects
CUI: C0018798
Disease: Congenital Heart Defects
0.040 GeneticVariation BEFREE A66G and C524T polymorphisms of the methionine synthase reductase gene are associated with congenital heart defects in the Chinese Han population. 22057956 2011
Congenital Heart Defects
CUI: C0018798
Disease: Congenital Heart Defects
0.040 GeneticVariation BEFREE MTRR 66A>G polymorphism in relation to congenital heart defects. 17087642 2006