Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs659366 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs17107315 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 40
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs1805094 0.716 0.440 1 65610269 missense variant G/C;T snv 0.16; 4.0E-06 16
rs2241767 0.763 0.440 3 186853407 intron variant A/G snv 0.10 10
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs1275561861 0.672 0.360 6 29944350 missense variant G/A snv 23
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15