Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267606841 0.882 0.120 2 165749801 missense variant A/C snv 5
rs7076156 0.925 0.120 10 62655424 missense variant A/C;G snv 0.80 3
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
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
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs150924946 0.882 0.120 1 156135271 missense variant A/G snv 4.8E-04 1.6E-04 5
rs3862434 1.000 0.080 15 90537155 intron variant A/G snv 0.48 3
rs771065515 1 156115240 missense variant A/G snv 2.5E-05 7.0E-06 2
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs553668 0.807 0.160 10 111079821 3 prime UTR variant A/G;T snv 8
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1799904 1.000 0.080 5 96429259 missense variant C/A;T snv 4.0E-06; 2.1E-03 2
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs2059806 0.807 0.240 19 7166365 synonymous variant C/G;T snv 4.0E-06; 0.26 7
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs2016520 0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16