Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1036199 0.925 0.160 5 157104725 missense variant C/A snv 0.87 0.83 3
rs10892279 1.000 0.120 11 118741072 intron variant G/A;T snv 0.25 3
rs1126407 0.925 0.200 1 236537507 missense variant T/A snv 0.61 0.61 3
rs13031237
REL
1.000 0.120 2 60908994 intron variant G/T snv 0.25 3
rs147846074 0.925 0.200 21 44289743 missense variant C/G;T snv 1.2E-05; 3.2E-05; 4.0E-06 3
rs150240657 0.925 0.120 11 47682026 missense variant G/A snv 8.7E-05 3.6E-04 3
rs1953126 1.000 0.120 9 120878222 intron variant T/C snv 0.68 3
rs34933034
CSK
0.925 0.120 15 74787133 intron variant G/A;T snv 3
rs7573065 1.000 0.120 2 218381984 upstream gene variant C/A;T snv 3
rs11586238 0.925 0.160 1 116720516 regulatory region variant C/G snv 0.19 4
rs11676922 0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs1310182 0.882 0.360 1 113830881 intron variant A/C;G snv 0.56 4
rs13315591 0.925 0.160 3 58571114 intron variant T/C snv 0.15 4
rs13447 0.882 0.200 7 75166663 non coding transcript exon variant T/A;C snv 1.9E-02 4
rs201802880 0.882 0.200 7 74779296 missense variant G/A snv 1.1E-03 4
rs212389 0.925 0.160 6 159068759 non coding transcript exon variant G/A snv 0.60 4
rs26232 0.925 0.160 5 103261019 intron variant C/T snv 0.30 4
rs3890745 0.925 0.200 1 2622185 intron variant T/C snv 0.40 4
rs6859219 0.925 0.160 5 56142753 intron variant C/A snv 0.20 4
rs864537 0.925 0.200 1 167442147 intron variant A/G snv 0.29 4
rs874040 0.925 0.160 4 26106575 downstream gene variant G/C snv 0.29 4
rs906868 0.925 0.120 2 30225478 intergenic variant G/T snv 0.53 4
rs934734 0.925 0.160 2 65368452 intron variant G/A;T snv 0.54 4
rs945635 0.882 0.200 1 157700500 5 prime UTR variant C/A;G snv 5.6E-05; 0.45 4
rs1800520 0.851 0.200 21 44290023 missense variant C/A;G;T snv 0.14; 8.3E-06 5