Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1282382243 0.807 0.120 13 50843630 missense variant G/A snv 8
rs1403934301 0.882 0.120 17 7631317 missense variant G/A snv 3
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 66
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 24
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 201
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 34
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 230
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 127
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 117
rs185847354 0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs20551 0.752 0.320 22 41152004 missense variant A/G snv 0.31 0.23 10
rs2066714 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 11
rs2075291 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 12
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 48
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 100
rs2536512 0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 36
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 22