Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6489785 1.000 0.040 12 120925921 TF binding site variant T/C snv 0.68 3
rs11264339 1.000 0.040 1 155168172 downstream gene variant C/T snv 0.56 2
rs2380205 0.882 0.080 10 5844771 upstream gene variant C/T snv 0.47 2
rs2452877 1.000 0.040 5 4027643 regulatory region variant A/G snv 0.60 2
rs2597513 1.000 0.040 3 13514336 regulatory region variant C/T snv 0.88 2
rs2726034 1.000 0.040 16 28325561 downstream gene variant T/C snv 0.37 2
rs3893384 1.000 0.040 15 79680713 regulatory region variant C/T snv 0.50 2
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 2
rs563697 1.000 0.040 2 118656877 intergenic variant A/G snv 0.25 2
rs7929543 0.925 0.120 11 49329474 intron variant A/C snv 0.12 2
rs10004892 1.000 0.040 4 188951696 intergenic variant T/C snv 0.21 1
rs10006108 1.000 0.040 4 97002862 intergenic variant C/T snv 0.48 1
rs10019259 1.000 0.040 4 95825984 intergenic variant C/A;T snv 1
rs10027671 1.000 0.040 4 153056676 intron variant G/A snv 0.35 1
rs10029800 1.000 0.040 4 152071589 intergenic variant C/A snv 0.63 1
rs10039512 1.000 0.040 5 68847366 intron variant C/G;T snv 1
rs10040260 1.000 0.040 5 1749100 intergenic variant C/A;G snv 1
rs10041756 1.000 0.040 5 22996131 intergenic variant G/A snv 0.14 1
rs10052628 1.000 0.040 5 25949752 intergenic variant C/T snv 7.8E-02 1
rs10053503 1.000 0.040 5 104778862 intron variant T/G snv 8.3E-02 1
rs10053765 1.000 0.040 5 99658228 intergenic variant T/C snv 0.49 1
rs10064843 1.000 0.040 5 25948342 regulatory region variant G/A snv 0.17 1
rs10067455 1.000 0.040 5 88162105 intergenic variant G/T snv 0.82 1
rs10069142 1.000 0.040 5 115777468 upstream gene variant A/G;T snv 1
rs1007126 1.000 0.040 20 51252774 intergenic variant A/G snv 0.34 1