Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs40401 0.776 0.440 5 132060785 missense variant C/T snv 0.29 0.33 8
rs4505848 0.776 0.400 4 122211337 intron variant A/G snv 0.29 8
rs9272346 0.790 0.320 6 32636595 intron variant G/A snv 0.54 8
rs1738074 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 9
rs367732974
F7
0.790 0.360 13 113105788 5 prime UTR variant G/A snv 8.9E-05 2.8E-05 9
rs2305480 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 10
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 10
rs549858786 0.790 0.320 2 112836807 5 prime UTR variant T/A snv 10
rs549908 0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29 10
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs563558831 0.776 0.320 19 40991226 upstream gene variant T/C snv 7.0E-06 11
rs6908425 0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs1063320 0.752 0.360 6 29830972 3 prime UTR variant C/G;T snv 12
rs1805010 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 12
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs2855812 0.790 0.360 6 31504943 intron variant G/T snv 0.23 13
rs562962093 0.742 0.520 10 52771740 upstream gene variant T/C snv 7.0E-06 13
rs7044343 0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs7528684 0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 13
rs2397084 0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs396991 0.742 0.480 1 161544752 missense variant A/C;G;T snv 0.33; 4.1E-06 14
rs721917 0.752 0.360 10 79946568 missense variant A/G snv 0.47 0.42 14