Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1352010373 0.641 0.560 17 75489265 splice acceptor variant G/C snv 73
rs1554700718 0.658 0.360 9 83975540 non coding transcript exon variant T/C snv 59
rs1554333853 0.689 0.320 7 40046006 missense variant A/G snv 54
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs1364709483 0.701 0.360 17 61400235 missense variant G/A snv 6.5E-05 36
rs1060499548 0.724 0.440 9 130872961 missense variant G/A snv 27
rs1801198 0.677 0.400 22 30615623 missense variant G/A;C snv 5.6E-05; 0.57 26
rs142239530 0.790 0.320 11 4091328 missense variant C/G;T snv 4.4E-05 24
rs121908557 0.752 0.280 17 63957514 missense variant C/T snv 8.2E-06 1.4E-05 23
rs1555429629 0.763 0.200 15 40729632 missense variant G/A snv 23
rs387906846 0.807 0.280 1 26773716 stop gained C/G;T snv 19
rs1553154130 0.807 0.280 1 8358231 missense variant T/A;C snv 18
rs1553284997 0.790 0.400 1 92833544 splice acceptor variant G/C snv 17
rs912001256 0.851 0.240 17 63947062 stop gained G/A snv 17
rs759125480 0.827 0.160 5 123377409 stop gained G/A snv 1.6E-05 16
rs149830411 0.827 0.360 17 46171276 stop gained G/A snv 5.2E-05 5.6E-05 15
rs730881014 0.776 0.360 1 155904494 stop gained A/C;G;T snv 15
rs141322087 0.851 0.160 11 17404552 missense variant C/T snv 1.2E-05 2.1E-05 13
rs2277923 0.752 0.160 5 173235021 synonymous variant T/C snv 0.41 0.44 13
rs267607079 0.776 0.240 2 39022772 missense variant C/A;G snv 13