Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 3
rs7216389 0.732 0.440 17 39913696 intron variant C/T snv 0.60 3
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 5
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 6
rs2305480 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 7
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 2
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 2
rs2290400 0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
rs4794820 0.790 0.160 17 39933091 intron variant A/G;T snv 3
rs8076131 0.790 0.200 17 39924659 intron variant G/A;C snv 3
rs9303277 0.790 0.240 17 39820216 intron variant C/T snv 0.52 4
rs12603332 0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 3
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs928413 0.807 0.120 9 6213387 upstream gene variant G/A;C snv 2
rs10445308 0.851 0.240 17 39781794 intron variant C/T snv 0.38 3
rs11557467 0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45 4
rs204993 0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 3
rs4795405 0.851 0.160 17 39932164 intron variant T/A;C snv 3
rs1888909 0.882 0.200 9 6197392 downstream gene variant T/A;C snv 2
rs2305479 0.882 0.160 17 39905964 missense variant C/T snv 0.43 0.39 4
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 3
rs7219923 0.882 0.160 17 39918265 non coding transcript exon variant C/T snv 0.52 4
rs8069176 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 3