Variant: rs12411886 

    present in Gene: CNNM2
    present in Chromosome: 10
    Position on Chromosome: 102925542
    Alleles of this Variant: C/A

rs12411886 in CNNM2 gene and Coronary heart disease PMID 21378990 2011 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.

rs12411886 in CNNM2 gene and Intracranial Aneurysm PMID 20364137 2010 Genome-wide association study of intracranial aneurysm identifies three new risk loci.

rs12411886 in CNNM2 gene and Parkinson Disease PMID 19915575 2009 Genome-wide association study reveals genetic risk underlying Parkinson's disease.