Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs1239681664 0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs146292819 0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs4149313 0.763 0.240 9 104824472 missense variant T/C snv 9
rs532997003 0.882 0.040 9 104840464 missense variant T/C snv 2.0E-05 3
rs9282541 0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs908832 0.851 0.120 9 137018032 missense variant A/C;G snv 0.97 0.96 4
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2032582 0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs63751001 0.790 0.240 16 16159555 missense variant C/T snv 2.8E-05 13
rs72653706 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs11887534 0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs142677199
ACE
0.882 0.040 17 63479897 missense variant G/A;T snv 3.2E-05 4
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs761401927
ACE
0.882 0.040 17 63488704 missense variant G/A snv 9.1E-05 4
rs428785 0.882 0.040 21 26844276 missense variant C/A;G;T snv 1.3E-05; 0.70 0.78 3
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs185847354 0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63