Variant: rs587777929 

    present in Gene: CCT7
    present in Chromosome: 2
    Position on Chromosome: 73252803
    Alleles of this Variant: C/T

rs587777929 in CCT7 gene and MYOCARDIAL INFARCTION, SUSCEPTIBILITY TO PMID 24213632 2013 Dysfunctional nitric oxide signalling increases risk of myocardial infarction.