Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10758203 1.000 0.040 9 33421422 intergenic variant G/A;C snv 1
rs114928225 1.000 0.040 2 118692164 intergenic variant T/A snv 1.0E-02 1
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 1
rs116080888 1.000 0.040 6 32618459 intergenic variant C/A snv 1
rs116506680 1.000 0.040 6 29813272 upstream gene variant T/A;C;G snv 1
rs11855650 1.000 0.040 15 70139434 intergenic variant G/T snv 0.39 1
rs1394371 0.925 0.080 15 78432127 intergenic variant C/T snv 0.22 1
rs17078110 1.000 0.040 6 148185476 intergenic variant T/C snv 1.0E-02 1
rs184697115 1.000 0.040 5 16005668 intergenic variant A/G snv 6.3E-03 1
rs190996050 1.000 0.040 5 1048492 downstream gene variant T/C snv 5.7E-03 1
rs2006209 1.000 0.040 19 41589873 downstream gene variant C/T snv 0.16 1
rs2179920 1.000 0.040 6 33091097 downstream gene variant C/T snv 0.27 1
rs28516445 1.000 0.040 15 49667937 intergenic variant A/G snv 0.18 1
rs3094054 0.807 0.280 6 30365728 upstream gene variant G/A;T snv 1
rs3129763 0.827 0.280 6 32623148 TF binding site variant G/A snv 0.23 1
rs35201538 1.000 0.040 9 33422490 intergenic variant -/T;TT delins 1
rs4105144 0.827 0.160 19 40852719 intron variant T/C snv 1
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 1
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 1
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 1
rs59396197 1.000 0.040 2 139675756 intergenic variant G/A snv 9.1E-02 1
rs61176212 1.000 0.040 20 13654465 intergenic variant G/A snv 4.3E-03 1
rs3132610 0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 1
rs17038564 1.000 0.040 2 65268924 3 prime UTR variant A/G snv 5.3E-02 1
rs7216064 1.000 0.040 17 67902693 intron variant G/A snv 0.22 1