Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10866713 1.000 0.080 5 159491886 intron variant G/A snv 0.16 1
rs10876994 0.925 0.120 12 57670954 upstream gene variant A/C;T snv 1
rs11129295 1.000 0.080 3 27747289 intergenic variant C/T snv 0.39 1
rs12048904 1.000 0.080 1 100865980 intergenic variant T/C snv 0.48 1
rs12946510 0.851 0.160 17 39756124 downstream gene variant C/T snv 0.37 1
rs13192841 0.925 0.120 6 137646077 intergenic variant G/A snv 0.24 1
rs13333054 1.000 0.080 16 85977427 intron variant C/A;T snv 1
rs1356122 1.000 0.080 3 154465773 intergenic variant G/A;C snv 1
rs1401884 1.000 0.080 16 85979945 intron variant G/C snv 0.18 1
rs1438131 1.000 0.080 2 23283911 regulatory region variant G/A snv 0.34 1
rs1449263 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 1
rs1610630 1.000 0.080 6 29761509 intron variant C/T snv 0.81 1
rs1633069 1.000 0.080 6 29756424 intron variant C/G snv 0.81 1
rs1633070 1.000 0.080 6 29756370 intron variant T/A;C snv 1
rs17066096 1.000 0.080 6 137131771 intergenic variant A/G snv 0.20 1
rs1737060 1.000 0.080 6 29765192 upstream gene variant G/C snv 0.79 1
rs1737068 1.000 0.080 6 29763146 non coding transcript exon variant C/A snv 0.81 1
rs17445836 0.851 0.320 16 85984057 intron variant G/A snv 0.15 1
rs2157082 1.000 0.080 6 32792937 intergenic variant G/A;C;T snv 1
rs233100 1.000 0.080 1 85306326 intron variant G/A snv 0.40 1
rs2516460 1.000 0.080 6 31450923 intron variant T/A;C;G snv 0.54 1
rs2523485 1.000 0.080 6 31383258 upstream gene variant T/C snv 0.87 1
rs2523638 1.000 0.080 6 31376496 upstream gene variant T/C snv 0.45 1
rs2530709 1.000 0.080 6 30972792 intergenic variant G/A;C;T snv 1
rs2530710 1.000 0.080 6 30972610 intergenic variant T/C snv 0.86 1