rs6922269, MTHFD1L

N. diseases: 7
Disease: Acute Coronary Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
0.020 GeneticVariation BEFREE We analyzed the relationship between rs6922269 variant on MTHFD1L gene and (i) risk of the acute coronary syndrome (ACS) in the Czech population and (ii) mortality in 7 years follow up. 25809277 2015
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
0.020 GeneticVariation BEFREE Genetic polymorphism rs6922269 in the MTHFD1L gene is associated with survival and baseline active vitamin B12 levels in post-acute coronary syndromes patients. 24618918 2014