Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs13003464 0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs3197999 0.732 0.280 3 49684099 missense variant G/A snv 0.26 0.27 6
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 5
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 5
rs11190140 0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55 4
rs11584383 0.827 0.200 1 200966738 downstream gene variant T/C snv 0.24 4
rs1736135 0.851 0.160 21 15432901 intron variant T/C snv 0.33 4
rs2188962 0.882 0.160 5 132435113 intron variant C/T snv 0.29 4
rs2301436 0.752 0.320 6 167024500 intron variant C/T snv 0.42 4
rs3764147 0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 4
rs9286879 0.851 0.200 1 172893094 intron variant A/G snv 0.32 4
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 3
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 3
rs11175593 0.882 0.160 12 40208138 non coding transcript exon variant C/T snv 2.8E-02 3
rs11465804 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 3
rs11747270 0.790 0.240 5 150879305 intron variant A/G snv 0.21 3
rs1456893 0.851 0.160 7 50230076 intron variant G/A snv 0.69 3
rs1551398 0.882 0.160 8 125527809 intron variant G/A snv 0.48 3
rs17582416 0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31 3
rs1847472 0.807 0.200 6 90263440 intron variant C/A snv 0.25 3
rs2274910 0.827 0.200 1 160882256 non coding transcript exon variant T/C snv 0.65 0.58 3