Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs2036527 0.851 0.080 15 78559273 regulatory region variant G/A snv 0.29 12
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 11
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 11
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 8
rs4769793 0.807 0.120 13 29985289 intergenic variant G/C snv 8
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 7
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 7
rs4415084 0.827 0.080 5 44662413 upstream gene variant C/T snv 0.49 6
rs17296479 0.851 0.040 5 81411157 non coding transcript exon variant T/A snv 9.4E-02 5
rs2252586 0.882 0.040 7 54911231 intergenic variant C/T snv 0.27 5
rs9600079 0.925 0.080 13 73154002 intergenic variant G/T snv 0.46 5
rs1535989 0.925 0.080 13 105370372 intergenic variant A/G;T snv 4
rs1862214 0.882 0.080 19 32544943 intergenic variant G/A;C snv 4
rs565453 0.882 0.160 5 112849696 intron variant A/C;G snv 4
rs614367 0.882 0.080 11 69513996 intergenic variant C/T snv 0.14 4
rs6785617 0.882 0.120 3 172501054 downstream gene variant A/T snv 3.7E-02 4
rs7716600 0.925 0.080 5 44874903 regulatory region variant A/C;T snv 4