Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs1458038 0.925 0.120 4 80243569 intergenic variant C/T snv 0.23 10
rs16998073 0.925 0.120 4 80263187 upstream gene variant A/G;T snv 10
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs10759931 0.790 0.360 9 117701869 upstream gene variant G/A;T snv 9
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs1173771 5 32814922 regulatory region variant A/G snv 0.65 9
rs2972146 0.882 0.040 2 226235982 intergenic variant G/T snv 0.72 9
rs10033464 0.807 0.200 4 110799605 downstream gene variant T/G snv 0.86 8
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs12149545 0.851 0.080 16 56959249 upstream gene variant G/A snv 0.23 7
rs1327235 20 10988382 intron variant A/G snv 0.46 7
rs11646213 0.827 0.320 16 82609046 intergenic variant A/T snv 0.47 6
rs11953630 5 158418394 intergenic variant C/A;T snv 6
rs13149993 4 80237391 regulatory region variant G/A;C snv 6
rs1887320 20 10985350 intron variant G/A snv 0.46 6