Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs35705950 0.763 0.240 11 1219991 splice region variant G/A;T snv 14
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 10
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 10
rs951005 0.807 0.200 9 34743684 intron variant G/A snv 0.78 10
rs6590330 0.851 0.280 11 128441164 intergenic variant G/A;T snv 5
rs12630450 1.000 0.160 3 169762416 downstream gene variant A/G snv 0.33 2
rs2672794 1.000 0.040 11 1219775 intron variant T/C snv 0.70 2
rs7633750 1.000 0.160 3 169791456 upstream gene variant G/A snv 0.38 2
rs1033198 11 1325572 intergenic variant T/A;C;G snv 1
rs10751635 11 1062990 intergenic variant A/G snv 0.41 1
rs10794278 11 1061718 intergenic variant G/T snv 0.32 1
rs10794279 11 1061781 intergenic variant C/T snv 0.32 1
rs10794280 11 1062867 intergenic variant C/T snv 0.30 1
rs10794284 11 1067011 intergenic variant G/A snv 0.34 1
rs10902073 11 1060934 TF binding site variant C/A snv 0.31 1
rs11858744 15 85339833 regulatory region variant C/T snv 0.40 1
rs12417955 11 1262997 downstream gene variant A/G snv 0.55 0.54 1
rs1453184 15 40437201 upstream gene variant A/G snv 0.59 1
rs1997392 3 169791864 upstream gene variant C/T snv 0.33 1
rs2301160 11 1063767 intergenic variant T/C snv 0.41 1
rs2334659 11 1335833 non coding transcript exon variant G/A snv 0.11 1
rs3129868 6 32436600 upstream gene variant A/C snv 0.89 1
rs4077759 11 1112068 downstream gene variant C/T snv 0.53 1
rs6974373 7 99993270 upstream gene variant C/A;G snv 1