Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs7831697 0.724 0.240 8 137124061 regulatory region variant T/A;C;G snv 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
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 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
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 10
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 9
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
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 8
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 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