Disease: Myocardial Infarction
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs117714106 0.882 0.080 14 84338144 intergenic variant C/T snv 9.1E-03 3
rs17222842 0.882 0.120 13 30765980 downstream gene variant G/A snv 6.1E-02 3
rs1722842 0.925 0.080 15 23785809 intron variant T/C snv 0.16 2
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs1870634 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 4
rs201052613 0.882 0.080 1 173026503 intron variant T/-;TT delins 9.4E-03 3
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs7136716 0.851 0.080 12 7538538 regulatory region variant A/G snv 0.22 6
rs7213516 0.882 0.080 17 63474189 upstream gene variant G/A snv 5.7E-02 3
rs9982601 0.851 0.080 21 34226827 intron variant C/T snv 0.15 4
rs1239681664
ABCA1
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs72653706
ABCC6
0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs514659
ABO
0.882 0.120 9 133266790 intron variant C/A;T snv 10