Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1016343 0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 8
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1050450 0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057941 0.701 0.280 1 155216951 non coding transcript exon variant G/A;T snv 0.46 18
rs1058808 0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131445 0.724 0.440 15 81309441 3 prime UTR variant T/A;C snv 16
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1143627 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 47
rs11536889 0.658 0.560 9 117715853 3 prime UTR variant G/C snv 0.11 27
rs11556218 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs125701 0.790 0.160 3 9748794 upstream gene variant G/A snv 0.13 7
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79