Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10806425 0.851 0.280 6 90216893 intron variant C/A snv 0.33 5
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs11676922 0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs11712165 0.882 0.200 3 119399949 intron variant T/G snv 0.30 5
rs1250552 0.882 0.200 10 79298270 intron variant A/C;G snv 5
rs12928822 0.882 0.200 16 11310036 intron variant C/T snv 0.13 5
rs13003464 0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs13010713 0.882 0.200 2 181131318 intron variant A/C;G snv 5
rs13098911 0.882 0.200 3 46193709 intron variant C/G;T snv 5
rs13151961 0.827 0.200 4 122194347 intron variant A/G snv 0.11 5
rs13315591 0.925 0.160 3 58571114 intron variant T/C snv 0.15 4
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs17035378 0.882 0.200 2 68371823 intron variant T/A;C snv 5
rs17810546 0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs26232 0.925 0.160 5 103261019 intron variant C/T snv 0.30 4
rs2816316 0.882 0.200 1 192567683 intron variant C/A snv 0.79 5
rs296547 0.882 0.200 1 200923009 intron variant T/C snv 0.53 5
rs3093023 0.851 0.160 6 167120802 intron variant G/A snv 0.34 4
rs3761847 0.827 0.200 9 120927961 intron variant G/A snv 0.52 4
rs4648356 1.000 0.080 1 2792599 intron variant C/A snv 0.39 3
rs4675374 0.882 0.200 2 203937855 intron variant T/C snv 0.65 5
rs4810485 0.732 0.480 20 46119308 intron variant T/A;G snv 4
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 4
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17