Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1554317002 0.724 0.440 7 39950821 frameshift variant C/- delins 45
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs1799946 0.732 0.360 8 6877909 5 prime UTR variant C/T snv 0.36 0.41 13
rs11362 0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 13
rs1800875 0.742 0.360 14 24510132 upstream gene variant C/T snv 0.41 12
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 12
rs324011 0.742 0.360 12 57108399 intron variant C/T snv 0.32 12
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs12153855 0.776 0.320 6 32107027 intron variant T/C snv 0.11 11
rs1805011 0.776 0.320 16 27362551 missense variant A/C;G;T snv 0.13; 1.2E-04; 3.6E-05 8
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs2248359 0.790 0.400 20 54174979 upstream gene variant C/T snv 0.47 8
rs569108 0.790 0.200 11 60095631 missense variant A/G snv 4.7E-02 7.3E-02 8
rs1295685 0.790 0.160 5 132660753 3 prime UTR variant A/G snv 0.81 7
rs138726443 0.790 0.200 1 152307547 stop gained G/A;C;T snv 2.8E-03; 4.0E-06; 1.6E-05 7
rs13199524 0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 9
rs28665122 0.807 0.240 15 101277522 upstream gene variant C/T snv 0.24 7
rs893051 0.807 0.400 3 190321812 intron variant G/A;C snv 7
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 18
rs12198173 0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs3745367 0.827 0.200 19 7669625 intron variant G/A snv 0.39 8
rs10249788 0.827 0.160 7 17298523 intron variant C/G;T snv 6
rs11584340 0.827 0.200 1 152313454 missense variant G/A snv 0.27 0.19 5
rs150597413 0.827 0.160 1 152305146 stop gained G/A;C;T snv 3.6E-05; 4.0E-06; 1.5E-03 5
rs167769 0.827 0.280 12 57109992 5 prime UTR variant C/T snv 0.31 5