Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs4648068 0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 97
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 103
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 93
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs1800449
LOX
0.641 0.400 5 122077513 missense variant C/A;T snv 4.0E-06; 0.17 33
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 55
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1051740 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs2424913 0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1801200 0.790 0.200 17 39723335 missense variant A/G;T snv 7
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205