Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2305480 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 7
rs2290400 0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 6
rs11557467 0.851 0.200 17 39872381 missense variant G/T snv 0.45 0.45 4
rs2305479 0.882 0.160 17 39905964 missense variant C/T snv 0.43 0.39 4
rs7219923 0.882 0.160 17 39918265 non coding transcript exon variant C/T snv 0.52 4
rs9303277 0.790 0.240 17 39820216 intron variant C/T snv 0.52 4
rs9303281 0.882 0.160 17 39917793 non coding transcript exon variant G/A snv 0.50 4
rs3859192 0.925 0.080 17 39972395 intron variant C/T snv 0.42 3
rs4794820 0.790 0.160 17 39933091 intron variant A/G;T snv 3
rs4795400 0.925 0.080 17 39910767 intron variant C/T snv 0.36 3
rs4795405 0.851 0.160 17 39932164 intron variant T/A;C snv 3
rs8069176 0.882 0.080 17 39900944 downstream gene variant G/A;T snv 3
rs8076131 0.790 0.200 17 39924659 intron variant G/A;C snv 3
rs907092 0.925 0.080 17 39766006 synonymous variant G/A snv 0.41 0.36 3
rs3894194 0.882 0.120 17 39965740 missense variant G/A snv 0.46 0.41 2
rs3902025 0.925 0.080 17 39963001 intron variant G/T snv 0.56 2
rs4795408 0.925 0.080 17 39951374 upstream gene variant G/A snv 0.41 2
rs6503525 0.925 0.080 17 39938921 intron variant G/A;C snv 2
rs6503526 0.925 0.080 17 39958345 intron variant C/T snv 0.41 2
rs8079416 0.925 0.080 17 39936460 intron variant T/C snv 0.45 2