Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1648707 0.925 0.080 3 186833922 intergenic variant A/C snv 0.43 3
rs2650000 0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs3093105 0.925 0.080 19 15897578 missense variant A/C snv 0.16 0.18 2
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1169288 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs10118757 0.827 0.120 9 21853340 intron variant A/G snv 0.26 7
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1333042 0.827 0.120 9 22103814 intron variant A/G snv 0.63 7
rs147377392 0.763 0.120 20 23048144 missense variant A/G snv 1.0E-04 2.8E-04 11
rs17114036 0.851 0.120 1 56497149 intron variant A/G snv 0.11 5
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs2576178 0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 9