rs72653706, ABCC6

N. diseases: 32
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
0.710 GeneticVariation BEFREE Our new c.3421C>T genotyping assays can be used for the rapid identification of this frequent mutation in PXE patients and of the recently newly proposed cardiac risk factor in young patients with myocardial infarcts of unknown origin. 14631379 2004
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
0.710 CausalMutation CLINVAR