Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13375144 1.000 0.040 1 196872560 intron variant C/T snv 0.22 1
rs13375150 1.000 0.040 1 196872709 intron variant C/T snv 0.22 1
rs13375236 1.000 0.040 1 196873141 intron variant C/T snv 0.22 1
rs16840607 1.000 0.040 1 196853900 intron variant T/G snv 0.34 1
rs16840639 0.925 0.120 1 196855643 intron variant T/C snv 0.23 1
rs17050244 1.000 0.040 2 120525054 regulatory region variant A/C;G snv 1
rs1738740 1.000 0.040 1 196839510 intergenic variant A/T snv 0.61 1
rs17573790 1.000 0.040 1 196640266 intergenic variant A/C snv 6.9E-02 1
rs1789110 0.925 0.040 18 77147088 regulatory region variant C/A snv 0.63 1
rs2133138 1.000 0.040 1 196874041 intron variant G/A snv 0.22 1
rs2336502 1.000 0.040 1 196873444 intron variant T/C snv 0.39 1
rs2336503 1.000 0.040 1 196874290 intron variant C/A snv 0.22 1
rs2842992 0.925 0.040 6 159650127 intron variant G/A snv 0.73 1
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 1
rs395998 1.000 0.040 1 196770707 upstream gene variant C/T snv 0.61 1
rs402032 1.000 0.040 1 196749084 downstream gene variant C/G snv 6.5E-02 1
rs4751889 1.000 0.040 10 122372672 upstream gene variant T/C snv 0.41 1
rs503002 1.000 0.040 1 196851157 intron variant A/G snv 0.66 1
rs6428363 1.000 0.040 1 196874581 intron variant G/A snv 0.39 1
rs6428364 1.000 0.040 1 196874919 intron variant C/T snv 0.21 1
rs6428365 1.000 0.040 1 196875001 intron variant C/A snv 0.21 1
rs6428366 1.000 0.040 1 196875037 intron variant A/G snv 0.21 1
rs6428367 1.000 0.040 1 196875062 intron variant T/C snv 0.21 1
rs6428368 1.000 0.040 1 196875180 intron variant T/C snv 0.19 1
rs6428369 1.000 0.040 1 196875205 intron variant T/C snv 0.23 1