Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs9834970 0.790 0.080 3 36814539 downstream gene variant T/C snv 0.45 9
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs6937506 0.807 0.280 6 132578260 intergenic variant G/A snv 0.25 7
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 7
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs12871532 0.851 0.040 13 108016199 intergenic variant T/C snv 0.46 5
rs13072940 0.851 0.040 3 36801132 regulatory region variant T/A snv 0.37 5
rs13418455 0.851 0.040 2 180212022 intergenic variant C/T snv 0.29 5
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs2769605 0.827 0.040 9 85297756 intergenic variant C/T snv 0.44 5
rs2839350 0.827 0.080 21 46597307 downstream gene variant G/A snv 0.22 5
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs6903874 0.851 0.080 6 132575771 downstream gene variant T/C snv 0.23 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 4
rs17066873 0.851 0.040 13 76889874 non coding transcript exon variant T/C snv 5.4E-02 4
rs17154917 0.851 0.040 7 81207393 intergenic variant G/A;T snv 4
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs221774 0.851 0.080 7 100701361 upstream gene variant A/G;T snv 4
rs3916966 0.882 0.080 13 105458546 upstream gene variant C/A snv 0.63 4
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 4