Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs1883832 0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 5
rs3761959 0.827 0.320 1 157699488 intron variant C/A;G;T snv 4
rs6074022 0.851 0.240 20 46111557 TF binding site variant C/G;T snv 3
rs4810485 0.732 0.480 20 46119308 intron variant T/A;G snv 3
rs1800693 0.776 0.360 12 6330843 non coding transcript exon variant T/C snv 0.36; 4.0E-06 0.38 3
rs6897932 0.683 0.560 5 35874473 missense variant C/T snv 0.23 0.21 2
rs704840 0.851 0.240 1 173257056 intergenic variant T/G snv 0.29 2
rs2300747 0.882 0.200 1 116561593 intron variant A/G snv 0.19 2
rs10168266 0.776 0.400 2 191071078 intron variant C/T snv 0.19 2
rs7601754 0.882 0.160 2 191075725 intron variant G/A;T snv 2
rs4149577 0.827 0.280 12 6338356 intron variant G/A;T snv 2
rs1150757 0.925 0.160 6 32061428 synonymous variant G/A;C snv 5.9E-02 2
rs28383224 0.925 0.160 6 32615876 regulatory region variant A/G snv 0.55 1
rs73366469 0.925 0.160 7 74619286 regulatory region variant T/C snv 0.12 1
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 1
rs3135388 0.807 0.240 6 32445274 downstream gene variant A/G snv 0.90 1
rs763780 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 1
rs117026326 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 1
rs9523762 0.925 0.120 13 92679633 intron variant G/A snv 0.39 1
rs703842 0.851 0.240 12 57768956 missense variant A/G snv 0.38 0.33 1
rs422951 0.807 0.280 6 32220606 missense variant T/C snv 0.40 0.40 1
rs1520333 0.925 0.120 8 78488803 intron variant A/G snv 0.40 1
rs10181656 0.763 0.360 2 191105153 intron variant G/C snv 0.79 1