Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1126772 0.851 0.320 4 87983034 3 prime UTR variant A/G snv 0.16 5
rs1128503 0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs11574944 1.000 0.200 16 30498669 intron variant C/T snv 0.25 1
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs11642873 0.851 0.280 16 85958099 intergenic variant A/C snv 0.15 4
rs116799036 1.000 0.200 6 31381371 downstream gene variant G/A snv 1
rs11755527 0.851 0.360 6 90248512 intron variant C/G snv 0.36 5
rs11769828 1.000 0.200 7 150534221 intergenic variant C/T snv 0.19 1
rs11792633 0.882 0.280 9 6248035 intron variant C/T snv 0.35 5
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs12119179 0.925 0.200 1 67281732 downstream gene variant A/C snv 0.30 2
rs12141431 1.000 0.200 1 67281340 downstream gene variant G/C snv 0.23 1
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121908147 0.807 0.280 1 247424041 missense variant G/A;C snv 8.3E-03; 4.0E-06 7
rs12212193 0.925 0.280 6 90287050 intron variant A/G snv 0.38 2
rs1234313 0.807 0.400 1 173197108 intron variant A/G snv 0.72 6
rs1234315 0.807 0.400 1 173209324 upstream gene variant C/T snv 0.57 6
rs12569232 0.882 0.280 1 211379722 intron variant G/C;T snv 4
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs12932187 0.925 0.320 16 10878023 intron variant C/G;T snv 2
rs1310182 0.882 0.360 1 113830881 intron variant A/C;G snv 0.56 4
rs13154629 1.000 0.200 5 96786754 non coding transcript exon variant C/T snv 0.16 1
rs13210247 0.882 0.280 6 111601517 non coding transcript exon variant A/G snv 0.10 3
rs1327295035 1.000 0.200 6 52187730 missense variant A/G snv 1
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9