Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs10680577 0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs10739971 0.882 0.080 9 94175398 intron variant G/A;C snv 5
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
rs12108497 0.851 0.080 4 184650403 intron variant C/G;T snv 6
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1229984 0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1305398818 0.925 0.080 4 88131886 missense variant G/A;C snv 4.0E-06; 4.0E-06 4
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
rs1447295 0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs144779807 0.827 0.120 5 1268529 missense variant C/A;T snv 4.0E-06; 4.0E-05 7
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1550117 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs1569686 0.752 0.400 20 32779273 intron variant G/A;C;T snv 15
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33