Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 11
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 7
rs1544210 0.882 0.240 10 92728044 regulatory region variant G/A snv 0.39 3
rs140485756 1.000 0.120 6 69410439 intergenic variant T/C snv 3.2E-02 2
rs2910397 1.000 0.120 19 47894860 intergenic variant C/T snv 0.38 2
rs56949836 1.000 0.120 9 90167763 intergenic variant C/T snv 8.9E-02 2
rs7312770 0.925 0.120 12 56073803 upstream gene variant C/T snv 0.53 2
rs74585555 1.000 0.120 2 81214976 intergenic variant G/A snv 4.9E-02 2
rs10739076 1.000 0.120 9 5440589 upstream gene variant A/C;T snv 1
rs10760321 1.000 0.120 9 124101917 TF binding site variant A/G snv 0.30 1
rs12460989 1.000 0.120 19 4785155 non coding transcript exon variant T/G snv 0.11 1
rs4744370 1.000 0.120 9 94715511 intergenic variant C/T snv 0.46 1
rs6022786 1.000 0.120 20 53830764 upstream gene variant A/G snv 0.55 1
rs684846 1.000 0.120 3 183173176 downstream gene variant C/T snv 0.85 1
rs7218361 1.000 0.120 17 39569151 downstream gene variant A/G snv 0.97 1
rs7558302 1.000 0.120 2 43609548 TF binding site variant C/T snv 0.59 1
rs7574059 1.000 0.120 2 123613428 intergenic variant G/A;C;T snv 1
rs8006998 1.000 0.120 14 75234687 downstream gene variant C/A;T snv 1
rs8013918 1.000 0.120 14 75242863 intron variant T/C snv 0.59 1
rs8013942 1.000 0.120 14 75244800 intron variant C/T snv 0.55 1
rs804279 1.000 0.120 8 11766380 upstream gene variant A/T snv 0.72 1