present in Gene: MIAT
present in Chromosome: 22
Position on Chromosome: 26662857
Alleles of this Variant: C/T
rs2331291 in
MIAT gene and
Myocardial Infarction
PMID 17066261 2006 Following linkage disequilibrium (LD) mapping, haplotype analyses revealed that six SNPs in this locus, all of which were in complete LD, showed markedly significant association with MI (chi2=25.27, P=0.0000005; comparison of allele frequency, 3,435 affected individuals versus 3,774 controls, in the case of intron 1 5,338 C>T; rs2331291).