Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs1438673 0.882 0.120 5 111131801 downstream gene variant C/T snv 0.61 4
rs17294280 0.882 0.120 15 67175947 intron variant A/G snv 0.19 4
rs3853750 0.882 0.160 5 110818610 intergenic variant T/C snv 0.30 3
rs10197862 0.925 0.120 2 102350089 intron variant A/G snv 0.18 2
rs11049300 0.925 0.120 12 28042192 intergenic variant A/G snv 2.5E-02 2
rs12450323 0.925 0.120 17 39816455 intron variant G/T snv 0.18 2
rs17513503 0.882 0.120 5 110810746 intergenic variant C/A;G snv 2
rs41295115 0.925 0.120 10 6082658 regulatory region variant T/C snv 4.8E-02 2
rs4833095 0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 2
rs62026376 0.925 0.120 16 11134855 intron variant C/T snv 0.18 2
rs6982751 0.925 0.120 8 10955964 intron variant C/G;T snv 2
rs7009110 0.925 0.120 8 80379644 intron variant T/C snv 0.53 2
rs7212938 0.925 0.120 17 39966427 missense variant G/A;C;T snv 4.1E-04; 4.2E-06; 0.52 2
rs72699186 0.925 0.120 9 6175855 intergenic variant A/T snv 0.15 2
rs72766477 0.925 0.120 5 84611411 intergenic variant G/A snv 3.1E-02 2
rs7521681 0.925 0.120 1 107779913 intron variant G/A snv 0.15 2
rs76043829 0.925 0.120 2 217812863 intron variant G/A snv 7.4E-02 2
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 2
rs9273373 0.925 0.120 6 32658824 upstream gene variant A/G snv 0.57 2