Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397507444
rs397507444
0.030 GeneticVariation BEFREE The carrier of FVL, TT genotype of C677T, and CC genotype of A1298C polymorphisms may act as risk factors for ESRD. 19520684

2010

dbSNP: rs397507444
rs397507444
0.030 GeneticVariation BEFREE MTHFR A1298C polymorphism is associated with cardiovascular risk in end stage renal disease in North Indians. 17899317

2008

dbSNP: rs397507444
rs397507444
0.030 GeneticVariation BEFREE In this case-control, cross-sectional study the frequency of the MTHFR 677C --> T and the 1298A --> C polymorphism was compared between patients with hypertension-related chronic renal failure (n = 90), patients with essential hypertension without kidney injury (n = 90), and healthy individuals (n = 90) who were matched for age and gender. 16280279

2005