Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 20
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 17
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 11
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 10
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 9
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs1495965 0.790 0.280 1 67287825 intergenic variant C/T snv 0.55 8
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 7
rs2836878 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 7
rs56167332 0.807 0.160 5 159400761 intron variant C/A;T snv 7
rs7556897 0.807 0.120 2 227795396 intergenic variant C/G;T snv 7
rs1569328 0.827 0.120 14 75275048 upstream gene variant C/T snv 0.12 6
rs1569723 0.851 0.280 20 46113425 upstream gene variant C/A snv 0.80 6
rs16967103 0.827 0.120 15 38606989 intergenic variant T/C snv 0.22 6