Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 20
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 9
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 9
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 9
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs103294 0.827 0.200 19 54293995 downstream gene variant T/C snv 0.82 7
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 7
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 7
rs17650792 0.827 0.080 3 49352817 downstream gene variant A/G snv 0.42 6
rs2410373 0.851 0.120 8 16066997 intergenic variant A/C snv 0.34 6
rs3136534 0.807 0.240 4 122448621 downstream gene variant T/G snv 0.29 6
rs9325782 0.851 0.120 8 16232964 intron variant C/T snv 0.87 6
rs406193 0.882 0.120 20 32811837 downstream gene variant T/C snv 0.91 5
rs9600079 0.925 0.080 13 73154002 intergenic variant G/T snv 0.46 5
rs11536858 0.851 0.240 9 117701869 upstream gene variant G/A;T snv 4
rs13083990 0.925 0.080 3 122295719 downstream gene variant T/C snv 0.30 4
rs565453 0.882 0.160 5 112849696 intron variant A/C;G snv 4
rs5759167 0.851 0.160 22 43104206 TF binding site variant G/T snv 0.40 4
rs6983269 0.925 0.080 8 2741967 intron variant C/A;G;T snv 0.42 4
rs11067228 0.925 0.080 12 114656455 downstream gene variant A/G snv 0.37 3
rs11228565 0.882 0.160 11 69211113 regulatory region variant G/A snv 0.16 3