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
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs841853 0.882 0.200 1 42935767 intron variant A/C snv 0.66 4
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs1043307 0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs1800783 0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs3764880 0.752 0.320 X 12906707 start lost A/G snv 0.31 0.30 11
rs13333226 0.827 0.200 16 20354332 intron variant A/G snv 0.23 10
rs4293393 0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs2053044 1.000 0.040 5 148825809 5 prime UTR variant A/G snv 0.59 5
rs758564400
REN
0.925 0.120 1 204156683 missense variant A/G snv 4.0E-06 5
rs9275224 0.851 0.200 6 32692101 TF binding site variant A/G snv 0.53 5
rs9974610 1.000 0.080 21 31646056 intergenic variant A/G snv 0.13 3
rs2856717 1.000 0.120 6 32702531 downstream gene variant A/G snv 0.64 2
rs3115573 1.000 0.120 6 32251066 upstream gene variant A/G snv 0.41 2
rs776400293 4 186076620 start lost A/G snv 4.0E-06 7.0E-06 1
rs9275424 6 32702799 downstream gene variant A/G snv 0.30 1
rs2248098
VDR
0.925 0.120 12 47859573 intron variant A/G;T snv 4
rs702553 0.882 0.160 5 60440946 intron variant A/T snv 0.37 6
rs11089788 0.851 0.120 22 36355056 intron variant C/A snv 0.46 5