Disease: Myocardial Infarction
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 9
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 8
rs2681472
ATP2B1
0.882 0.080 12 89615182 intron variant A/G snv 0.14 6
rs72743461
SMAD3
0.827 0.160 15 67149412 intron variant C/A;T snv 6
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 4
rs10738607
CDKN2B-AS1
0.925 0.080 9 22088095 intron variant A/G snv 0.42 3
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 3
rs28451064 0.925 0.080 21 34221526 intron variant G/A snv 9.2E-02 3
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 3
rs55791371
SMARCA4
0.925 0.080 19 11077477 intron variant A/C snv 0.11 3
rs16880442
ITGA1
0.925 0.080 5 52889863 non coding transcript exon variant G/A;T snv 2
rs180803
BCRP1 ; POM121L9P
0.925 0.080 22 24262890 intron variant G/A;T snv 2
rs1870634 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 2
rs2891168
CDKN2B-AS1
0.851 0.160 9 22098620 intron variant A/G snv 0.40 2
rs4593108 0.925 0.080 4 147359849 regulatory region variant C/G snv 0.31 2
rs72689147
GUCY1A1
0.925 0.080 4 155718736 intron variant G/T snv 0.15 2
rs9970807
PLPP3
0.925 0.080 1 56499992 intron variant C/T snv 0.11 2