Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 16
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 6
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs12365699 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 5
rs1444782 0.851 0.240 10 9016708 intergenic variant G/A snv 0.35 5
rs2025758 0.882 0.160 10 8799706 intergenic variant T/C snv 0.41 4
rs3853750 0.882 0.160 5 110818610 intergenic variant T/C snv 0.30 4
rs4722404 0.851 0.120 7 3089155 intron variant T/C snv 0.40 4
rs4982958 0.851 0.200 14 24518659 intergenic variant C/T snv 0.50 4
rs6594499 0.882 0.120 5 111134439 downstream gene variant C/A snv 0.56 4
rs7936562 0.882 0.160 11 76567214 intergenic variant T/C snv 0.59 4
rs976078 0.882 0.120 13 82963398 intron variant A/C snv 0.15 4
rs12634229 0.882 0.120 3 112657461 intergenic variant T/C snv 0.15 3
rs13277355 0.882 0.120 8 127765473 intergenic variant A/G snv 0.71 3
rs17389644 0.925 0.120 4 122576542 intergenic variant G/A;T snv 3
rs2390314 0.925 0.120 7 20416355 downstream gene variant A/C;T snv 3
rs4739738 0.882 0.120 8 80379410 intron variant G/A snv 0.60 3