Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs750805885 0.882 0.080 1 150579475 frameshift variant -/C delins 4.7E-06 3
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs769442590
LPL
0.925 0.040 8 19960927 missense variant A/C;G snv 1.6E-05 2
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs17465637 0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1008438 0.807 0.120 6 31815431 upstream gene variant A/C;T snv 6
rs2298566 0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06 5
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1927911 0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs5743810 0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 21