Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1002656 1.000 0.040 1 36727140 intergenic variant C/T snv 0.56 1
rs1008042 1.000 0.040 10 4583381 intergenic variant C/A;T snv 1
rs1014969 1.000 0.040 3 52774325 upstream gene variant G/A snv 0.44 1
rs1039197 1.000 0.040 10 4617005 intergenic variant A/C snv 0.71 1
rs10457592 1.000 0.040 6 99104094 intergenic variant G/A;T snv 1
rs10795187 1.000 0.040 10 4567598 intergenic variant G/A snv 0.28 1
rs10809385 1.000 0.040 9 11208995 intergenic variant C/A;T snv 1
rs10890045 1.000 0.040 1 73531941 intergenic variant T/C snv 0.66 1
rs10904290 1.000 0.040 10 4574670 intergenic variant A/G snv 8.4E-02 1
rs10904299 1.000 0.040 10 4603975 intergenic variant A/C snv 0.21 1
rs10904300 1.000 0.040 10 4606242 intergenic variant T/C snv 0.23 1
rs10904319 1.000 0.040 10 4699650 intergenic variant T/C snv 0.42 1
rs10959631 1.000 0.040 9 11220986 intergenic variant C/T snv 0.16 1
rs10959913 1.000 0.040 9 11544964 intergenic variant T/G snv 0.19 1
rs10959926 1.000 0.040 9 11553382 intergenic variant T/C snv 0.14 1
rs10960103 1.000 0.040 9 11699270 intron variant C/G;T snv 1
rs10994143 1.000 0.040 10 60021320 downstream gene variant A/G snv 5.2E-02 1
rs11033303 1.000 0.040 11 35849716 intergenic variant G/A;T snv 0.29 1
rs11124319 1.000 0.040 2 22212484 intron variant A/G snv 0.63 1
rs11135349 1.000 0.040 5 165096466 intron variant A/C snv 0.61 1
rs111945524 1.000 0.040 2 105482561 intergenic variant C/T snv 3.3E-02 1
rs11210111 1.000 0.040 1 73050889 intergenic variant C/A;T snv 1
rs11252607 1.000 0.040 10 4596451 intergenic variant G/A snv 0.22 1
rs11252615 1.000 0.040 10 4599964 intergenic variant C/T snv 0.48 1
rs11252622 1.000 0.040 10 4607844 intergenic variant C/T snv 0.26 1