Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs312262717 0.790 0.240 15 44659104 frameshift variant A/-;AA delins 18
rs1054442
DDN
0.925 0.040 12 48995537 3 prime UTR variant A/C snv 0.46 4
rs11152369 0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5
rs137928907 0.882 0.040 12 130827204 missense variant A/C snv 1.4E-02 1.5E-02 3
rs17673138 0.851 0.040 8 32840440 intron variant A/C snv 8.6E-02 4
rs4380187 0.925 0.040 2 184947213 intergenic variant A/C snv 0.34 3
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 15
rs12443954 0.851 0.040 16 89675088 intron variant A/C;G snv 5
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs10968749 0.851 0.040 9 28752486 intergenic variant A/G snv 5.5E-02 4
rs11191454 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs12576775 0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs1521470 0.925 0.040 7 45607253 intron variant A/G snv 0.89 2
rs17158930 0.851 0.040 7 111871082 intron variant A/G snv 0.25 4
rs17662626 0.851 0.040 2 193119895 intergenic variant A/G snv 5.9E-02 5
rs209474 0.925 0.040 6 32956807 intron variant A/G snv 0.38 2
rs2299682 0.882 0.040 20 9448697 intron variant A/G snv 9.1E-02 3
rs2997119 0.882 0.040 13 55819766 intergenic variant A/G snv 0.52 3
rs324899 0.925 0.040 5 88619764 intron variant A/G snv 0.97 2
rs4356203 0.925 0.040 11 17138601 intron variant A/G snv 0.31 4
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 4
rs548181 0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 5
rs61945387 0.882 0.040 12 117921609 intron variant A/G snv 7.7E-02 3
rs62173322 0.882 0.040 2 169754519 intron variant A/G snv 0.32 4
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5