Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7746082 0.851 0.160 6 105987394 regulatory region variant G/A;C snv 3
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs4263839 0.807 0.160 9 114804160 intron variant A/G snv 0.75 3
rs1551398 0.882 0.160 8 125527809 intron variant G/A snv 0.48 3
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs2188962 0.882 0.160 5 132435113 intron variant C/T snv 0.29 4
rs11167764 0.925 0.120 5 142099500 regulatory region variant A/C snv 0.80 2
rs11747270 0.790 0.240 5 150879305 intron variant A/G snv 0.21 3
rs1736135 0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 3
rs2274910 0.827 0.200 1 160882256 non coding transcript exon variant T/C snv 0.65 0.58 3
rs2301436 0.752 0.320 6 167024500 intron variant C/T snv 0.42 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs11584383 0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 4
rs6908425 0.752 0.320 6 20728500 intron variant T/C snv 0.78 3
rs3828309 0.882 0.160 2 233271764 intron variant A/G snv 0.42 3
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs11175593 0.882 0.160 12 40208138 non coding transcript exon variant C/T snv 2.8E-02 3
rs4613763 0.851 0.240 5 40392626 regulatory region variant T/C snv 0.14 3
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs3764147 0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 4
rs762421 0.851 0.360 21 44195678 intron variant G/A snv 3
rs3197999 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6