Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1050998 1.000 0.080 17 4735442 missense variant A/G snv 0.46 0.41 1
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1151640 1.000 0.080 1 247672648 missense variant T/C snv 0.46 0.36 1
rs4358188
BPI
0.827 0.160 20 38318446 missense variant G/A;C snv 0.46 7
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs12218 0.763 0.280 11 18269774 synonymous variant T/C snv 0.42 0.36 11
rs12794714 0.708 0.360 11 14892029 synonymous variant G/A snv 0.41 0.35 15
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs3737983 0.851 0.120 1 53250744 missense variant G/A;T snv 0.40; 2.4E-05; 1.2E-05 4
rs1376251 0.882 0.160 12 10986253 missense variant C/T snv 0.40 0.28 3
rs11614913 0.512 0.760 12 53991815 mature miRNA variant C/T snv 0.39 0.34 111
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs693 0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs9898 0.925 0.160 3 186672838 missense variant C/T snv 0.38 0.43 3
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs203462 0.807 0.200 17 19909228 missense variant T/C snv 0.37 0.43 7
rs17568 0.752 0.320 1 1212042 synonymous variant C/T snv 0.37 0.31 12
rs1024323 0.882 0.160 4 3004316 missense variant C/A;G;T snv 0.36 4
rs7447815 1.000 0.080 5 1240642 stop gained C/G;T snv 0.36; 7.6E-05 2
rs1053874 0.851 0.240 16 3657746 missense variant G/A;T snv 0.36; 4.0E-06 7
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106