Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10795945 1.000 0.080 10 12260608 intergenic variant T/A;C snv 2
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 5
rs11257655 1.000 0.080 10 12265895 TF binding site variant C/T snv 0.23 4
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 14
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 7
rs2191349 1.000 0.080 7 15024684 intergenic variant G/T snv 0.54 4
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 6
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 8
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs7020996 0.925 0.120 9 22129580 downstream gene variant C/A;T snv 3
rs7173964 1.000 0.080 15 62104743 regulatory region variant G/A snv 0.49 3
rs72892910 1.000 0.080 6 50849174 downstream gene variant G/T snv 0.17 2
rs7374732 1.000 0.080 3 23161963 regulatory region variant C/T snv 0.73 4
rs7923837 0.882 0.160 10 92722160 intergenic variant G/A;T snv 3
rs8089364 0.925 0.120 18 60191596 upstream gene variant T/C snv 0.21 6
rs11708067 0.882 0.080 3 123346931 intron variant A/G snv 0.19 6
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs2246012 1.000 0.080 6 131577068 intron variant T/A;C snv 2
rs4865796 1.000 0.080 5 53976834 intron variant G/A snv 0.72 3
rs6947395 1.000 0.080 7 69941675 intron variant A/T snv 0.20 2
rs12454712 0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs9891146 1.000 0.080 17 67991933 missense variant T/C snv 0.64 0.60 2
rs76895963 1.000 0.080 12 4275678 intron variant T/G snv 1.5E-02 6
rs2206734 0.882 0.160 6 20694653 intron variant C/T snv 0.20 4
rs35261542 1.000 0.080 6 20675561 intron variant C/A snv 0.26 3