Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE In addition, history of retinopathy was associated with the MTHFR C677T mutation in patients with DPN. 23901246

2013

dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE Four hundred and eighty adolescents were screened annually for retinopathy and microalbuminuria for a median of 4 yr. Molecular analysis for the polymorphisms 677C-->T, 1298A-->C in MTHFR, and 66A-->G in MTRR was performed. 18774994

2008

dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE The relationship between C677T methylenetetrahydrofolate reductase gene polymorphism and retinopathy in type 2 diabetes: a meta-analysis. 15902512

2005

dbSNP: rs1217691063
rs1217691063
0.040 GeneticVariation BEFREE One putative determinant of PAD is the 677C>T polymorphism in the gene encoding methylenetetrahydrofolate reductase (MTHFR), which has previously been found to associate with various diabetic complications including retinopathy, nephropathy, atherosclerosis and coronary heart disease. 16274479

2005