Disease: Myocardial Infarction
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800888
ADRB2
0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs1801058
GRK4
0.882 0.120 4 3037423 missense variant T/C;G snv 0.62 4
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1982073
TGFB1
0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs20455
KIF6 ; LOC107986594
0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs2057482
HIF1A-AS2 ; HIF1A-AS3 ; HIF1A
0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs2067853
AGT
0.851 0.160 1 230702512 downstream gene variant G/A snv 0.25 5
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs3135506
APOA5
0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs320
LPL
0.827 0.200 8 19961566 intron variant T/A;G snv 9
rs367732974
F7
0.790 0.360 13 113105788 5 prime UTR variant G/A snv 8.9E-05 2.8E-05 9
rs3732379
CX3CR1
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
rs3789679
AGT
0.925 0.120 1 230713948 intron variant G/A;T snv 4