Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs13003464 0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs17810546 0.827 0.440 3 159947262 intron variant A/G snv 8.2E-02 6
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs3748816 0.827 0.200 1 2595307 missense variant A/G snv 0.41 0.46 6
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 6
rs10806425 0.851 0.280 6 90216893 intron variant C/A snv 0.33 5
rs10903122 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 5
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 5
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
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
rs13314993 0.882 0.200 3 32973977 regulatory region variant G/C;T snv 5
rs17035378 0.882 0.200 2 68371823 intron variant T/A;C snv 5
rs1738074 0.790 0.320 6 159044945 5 prime UTR variant T/C snv 0.49 5
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
rs4675374 0.882 0.200 2 203937855 intron variant T/C snv 0.65 5
rs4819388 0.790 0.240 21 44227538 3 prime UTR variant T/C snv 5