Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1303946678 0.925 0.040 22 42126851 missense variant C/G snv 3
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1799998 0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs198358 0.925 0.040 1 11844019 3 prime UTR variant T/C snv 0.32 4
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2149954 0.882 0.080 5 158393594 intron variant C/T snv 0.37 5
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs5068 0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs9838915 0.882 0.120 3 126347377 intron variant G/A snv 0.19 4
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9943582 0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs1800888 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs1801252 0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38