rs3846662, HMGCR

N. diseases: 12
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 The LDL-associated SNP, rs3846662, appears to confer susceptibility to MI in Japanese. 20145341 2010