Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
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
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs9351814 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 4
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
rs12579302 0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
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
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs7632505 0.827 0.120 3 123019460 intron variant A/G snv 0.34 17
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs1799998 0.742 0.200 8 142918184 upstream gene variant A/G;T snv 0.38 14
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs7115242 0.851 0.120 11 117037567 intron variant A/G;T snv 16
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56