rs10118757, MTAP

N. diseases: 7
Disease: Myocardial Infarction ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.010 GeneticVariation BEFREE As reported previously, rs10118757 was not associated with MI in the current study. 23462334 2013