Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs72653706
rs72653706
ABCC6
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
dbSNP: rs72653706
rs72653706
ABCC6
A 0.710 CausalMutation CLINVAR