Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1227756 0.925 0.080 10 69828748 intron variant G/A;C snv 2
rs2710833 0.925 0.080 4 168488807 intron variant T/A;C snv 2
rs343064 0.925 0.080 7 35515178 upstream gene variant C/G;T snv 2
rs643608 0.925 0.080 21 43348682 intergenic variant C/T snv 0.69 2
rs6487679 0.925 0.080 12 9218736 intergenic variant C/T snv 0.80 2
rs6591182 0.925 0.080 11 65582285 missense variant T/G snv 0.47 0.45 2
rs887304 0.925 0.080 12 3648382 3 prime UTR variant T/C snv 0.77 2
rs2645424 0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs236918 0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs2896019 0.790 0.160 22 43937814 intron variant T/G snv 0.20 10
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs4374383 0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs1275561861 0.672 0.360 6 29944350 missense variant G/A snv 23
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs2241883 0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs17107315 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 40
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105