Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1805087
rs1805087
MTR
0.030 GeneticVariation BEFREE Mild hyperhomocysteinemia (P=0.05) in the probands was associated with rs1805087 'AA'. 28250422

2017
dbSNP: rs1805087
rs1805087
MTR
0.030 GeneticVariation BEFREE Further study is needed to confirm the role of HHcy and MS A2756G mutation in the development of hyperlipidemia. 19263808

2008
dbSNP: rs1805087
rs1805087
MTR
0.030 GeneticVariation BEFREE Mutations in methylenetetrahydrofolate reductase (C667T), cystathionine beta-synthase (T833C), and methionine synthase (A2756G) genes cause hyperhomocysteinemia, an independent risk factor for atherothrombosis. 12476935

2002