Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3751143 0.742 0.480 12 121184501 missense variant A/C;G snv 0.19; 4.0E-06 12
rs11225395 0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs1052053 1.000 0.080 1 156232382 missense variant A/C;G snv 1.0E-03; 0.38 3
rs2619112 0.882 0.160 17 4632090 intron variant A/C;G snv 4.0E-06; 0.53 3
rs397514465 0.925 0.280 5 59193507 missense variant A/C;G snv 3
rs434473 0.925 0.160 17 7001615 missense variant A/C;G snv 4.0E-06; 0.38 2
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs755449669 0.851 0.160 19 11111514 missense variant A/C;G;T snv 4.0E-06 5
rs1764390 0.882 0.160 1 34794360 missense variant A/C;G;T snv 0.61 0.69 3
rs7304841 1.000 0.080 12 20424659 intron variant A/C;G;T snv 2
rs1169288 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs8192284 0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs1271572 0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs2682818 0.742 0.320 12 80935757 non coding transcript exon variant A/C;T snv 0.83 14
rs9551963 0.851 0.160 13 30758410 intron variant A/C;T snv 6
rs762624 0.851 0.280 6 36677811 non coding transcript exon variant A/C;T snv 0.37; 2.4E-05 4
rs730012 1.000 0.080 5 179793637 upstream gene variant A/C;T snv 2
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63