Disease: Myocardial Infarction
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5985
F13A1
0.724 0.280 6 6318562 missense variant C/A;T snv 0.20; 2.4E-05 20
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs1042579
THBD
0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs767830104
CXCR4
0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs5888
SCARB1
0.752 0.200 12 124800202 synonymous variant A/G;T snv 0.59; 4.0E-06 11
rs57137919
ABCG1 ; LOC105372814
0.776 0.160 21 42218908 intron variant G/A snv 0.14 9
rs243866
MMP2
0.827 0.120 16 55477625 intron variant G/A snv 0.19 8
rs4746720
SIRT1
0.790 0.320 10 67917073 3 prime UTR variant T/C snv 2.4E-02 7
rs6003
F13B
0.851 0.240 1 197061891 missense variant C/T snv 0.88 0.76 5