Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2331291
rs2331291
Entrez Id: 440823
Gene Symbol: MIAT
MIAT
CUI: C0027051
Disease:
Myocardial Infarction
0.710 GeneticVariation BEFREE 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). 17066261 2006
dbSNP: rs2331291
rs2331291
Entrez Id: 440823
Gene Symbol: MIAT
MIAT
CUI: C0027051
Disease:
Myocardial Infarction
0.710 GeneticVariation GWASDB 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). 17066261 2006