rs1801133, MTHFR

N. diseases: 174
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.030 GeneticVariation BEFREE Associations of the MTHFR rs1801133 polymorphism with coronary artery disease and lipid levels: a systematic review and updated meta-analysis. 30115070 2018
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.030 GeneticVariation BEFREE The presence of the T allele of rs1801133 increases the odds of coro</span>nary atherosclerosis severity when associated with conventional risk factors. 23391848 2013
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
0.030 GeneticVariation BEFREE The rs1801133 polymorphism of the MTHFR gene affects risk of coronary artery disease. 22440940 2012