Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs115707823 0.701 0.320 6 30374976 intergenic variant G/A snv 19
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 7
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
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs9951150 0.851 0.040 18 55153893 intergenic variant A/G;T snv 5
rs13212562 0.925 0.120 6 27332531 intergenic variant A/G snv 0.13 4
rs6855246 1.000 0.040 4 102191313 intergenic variant A/G snv 0.14 4
rs10099100 8 10719265 downstream gene variant G/C snv 0.32 3
rs10149470 1.000 0.040 14 103551616 upstream gene variant A/G snv 0.54 3
rs11210892 1.000 0.040 1 43634413 intergenic variant G/A snv 0.51 3
rs2535627 1.000 0.040 3 52811089 downstream gene variant T/A;C;G snv 3
rs4380187 0.925 0.040 2 184947213 intergenic variant A/C snv 0.34 3
rs6940116 1.000 0.040 6 27740953 upstream gene variant A/G snv 0.18 3
rs7405404 0.925 0.040 16 13656002 intergenic variant T/A;C snv 3
rs911186 0.925 0.040 6 27182820 intergenic variant A/G snv 0.25 3
rs10791111 1.000 0.040 11 130986204 intergenic variant T/G snv 0.45 2
rs1080500 1.000 0.040 3 53141001 intergenic variant G/A snv 0.27 2
rs11223651 1.000 0.040 11 133971139 intergenic variant C/T snv 0.16 2
rs114041423 1.000 0.040 6 29639270 upstream gene variant G/A snv 2