Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs140226130 0.790 0.200 18 33336845 intron variant -/CTTTTTGCT delins 7.8E-02 8
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs9351814 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 4
rs144303414 1.000 0.040 18 48509413 intergenic variant A/C snv 1.5E-02 3
rs762151808 0.925 0.040 14 94378559 missense variant A/C snv 4.0E-06 7.0E-06 2
rs10927887 0.925 0.040 1 16024780 missense variant A/C;G snv 0.55 3
rs112434206 1.000 0.040 5 33083283 intron variant A/C;G snv 7.6E-03 3
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1801252 0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17