Disease: Myocardial Infarction
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5743708
TLR2
0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs708272
CETP
0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs1042579
THBD
0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs4746720
SIRT1
0.790 0.320 10 67917073 3 prime UTR variant T/C snv 2.4E-02 7
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157