Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2009746 1.000 0.040 15 78461760 intron variant A/G snv 0.29 4
rs2241718 0.882 0.040 19 41323701 3 prime UTR variant G/A snv 0.15 4
rs2656065 1.000 0.040 15 78458207 intron variant G/A snv 0.39 4
rs2955083 1.000 0.040 3 128242335 intron variant T/A snv 0.89 4
rs4243084 1.000 0.040 15 78619330 intron variant G/C snv 0.30 4
rs6837671 0.925 0.040 4 88951941 intron variant A/G snv 0.47 4
rs71636784 1.000 0.040 1 26842709 intron variant T/G snv 0.12 4
rs7180002 1.000 0.040 15 78581651 intron variant A/T snv 0.26 4
rs7181486 1.000 0.040 15 78449276 intron variant T/C snv 0.29 4
rs8042238 1.000 0.040 15 78481929 intron variant C/T snv 0.51 4
rs8042849 1.000 0.040 15 78525587 intron variant C/T snv 0.65 4
rs9399401 1.000 0.040 6 142347764 intron variant T/C snv 0.31 4
rs965604 1.000 0.040 15 78496881 intron variant G/A snv 0.50 4
rs10429950 1.000 0.040 1 218451191 intergenic variant T/C snv 0.33 3
rs10866659 1.000 0.040 5 157510035 intron variant A/G;T snv 3
rs114205691 1.000 0.040 15 78608771 intron variant C/A;T snv 3
rs11633958 1.000 0.040 15 78569722 intron variant C/A;T snv 3
rs11727735 1.000 0.040 4 105710713 intron variant A/G snv 4.4E-02 3
rs11771259 1.000 0.040 7 7237584 intron variant C/G snv 1.0E-01 3
rs11852372 1.000 0.040 15 78509052 intron variant A/C snv 0.27 3
rs11858836 1.000 0.040 15 78490935 intron variant G/A;T snv 3
rs12459249 1.000 0.040 19 40833991 intron variant T/C snv 0.66 3
rs12499182 1.000 0.040 4 144526904 intron variant G/A;C snv 3
rs12501071 1.000 0.040 4 144569207 intron variant C/T snv 0.42 3
rs12510916 1.000 0.040 4 144451096 intron variant C/T snv 0.25 3