Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 16
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 15
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 12
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 9
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 9
rs4324798 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 8
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 7
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 7
rs6457327 0.790 0.320 6 31106253 downstream gene variant A/C snv 0.66 7
rs1508595 0.851 0.240 12 88592239 intron variant G/A;T snv 5
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 5
rs4624820 0.851 0.240 5 142302223 regulatory region variant G/A snv 0.55 5
rs801114 0.827 0.120 1 228862088 downstream gene variant T/G snv 0.48 5
rs29232 0.925 0.240 6 29643654 intergenic variant C/T snv 0.39 4
rs305061 0.851 0.280 16 85942053 intron variant C/A;T snv 4
rs5759167 0.851 0.160 22 43104206 TF binding site variant G/T snv 0.40 4
rs710521 0.851 0.200 3 189928144 intergenic variant T/C snv 0.24 4