Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3846662
rs3846662
HMGCR
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		0.010 GeneticVariation BEFREE The LDL-associated SNP, rs3846662, appears to confer susceptibility to MI in Japanese. 20145341

2010