Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs20551 0.752 0.320 22 41152004 missense variant A/G snv 0.31 0.23 10
rs3135388 0.807 0.240 6 32445274 downstream gene variant A/G snv 0.90 7
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs4748793 0.851 0.120 10 22194082 intergenic variant A/G snv 0.18 4
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs6964969 0.851 0.120 7 50405553 downstream gene variant A/G snv 0.23 4
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs7809758 0.882 0.120 7 50505635 intron variant A/G snv 0.36 3
rs880028 0.882 0.120 7 50502438 intron variant A/G snv 0.21 3
rs9479
PML
0.851 0.120 15 74036235 3 prime UTR variant A/G snv 0.50 6
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2043211 0.653 0.480 19 48234449 missense variant A/T snv 0.33 0.29 29
rs6021191 0.851 0.120 20 51419700 intron variant A/T snv 4.9E-02 5
rs10740055 0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs1470755915 0.776 0.240 8 92005229 missense variant C/A snv 7.0E-06 10
rs7088318 0.851 0.120 10 22564019 intron variant C/A snv 0.55 4
rs927698341 0.776 0.240 8 92005280 synonymous variant C/A snv 4.0E-06 2.8E-05 10
rs1127354 0.667 0.400 20 3213196 missense variant C/A;G snv 7.5E-02 26
rs200890679 0.790 0.240 1 11795191 missense variant C/A;G snv 1.8E-04 2.0E-04 7
rs41320251 0.882 0.120 20 3213196 missense variant C/A;G snv 3
rs9400241 0.882 0.120 6 108682786 3 prime UTR variant C/A;G snv 4
rs2274407 0.882 0.120 13 95206781 missense variant C/A;G;T snv 9.7E-02 0.10 4
rs3731249 0.683 0.320 9 21970917 missense variant C/A;G;T snv 2.1E-02 23
rs35201683
HFE
0.732 0.360 6 26094205 stop gained C/A;T snv 1.4E-03 12