Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10914456 1.000 0.040 1 31622570 intron variant T/C snv 0.51 2
rs110402 0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs161645 1.000 0.040 5 104734216 intron variant A/G snv 0.77 2
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs2227631 0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2287161 0.827 0.080 12 106987362 upstream gene variant C/G;T snv 7
rs2535629 0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs33388 0.776 0.360 5 143317730 intron variant A/T snv 0.53 12
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs41423247 0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs4570625 0.724 0.200 12 71938143 upstream gene variant G/T snv 0.27 25
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6191 0.925 0.040 5 143278591 3 prime UTR variant C/A snv 0.48 4
rs6198 0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6994992 0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs7124442 0.827 0.160 11 27655494 3 prime UTR variant C/G;T snv 9
rs738499 0.851 0.120 22 41381096 intron variant G/T snv 0.76 9
rs776943620
ACE
0.851 0.120 17 63477287 missense variant G/A snv 2.1E-05 7