Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2523554 0.925 0.080 6 31364052 upstream gene variant C/T snv 0.70 5
rs12711490 0.925 0.080 16 85939422 intron variant T/C snv 0.18 4
rs2066807 0.925 0.080 12 56346898 missense variant C/G snv 4.9E-02 4.6E-02 4
rs638893 0.882 0.080 11 118827828 intergenic variant G/A snv 0.79 4
rs10276619 1.000 0.080 7 50273756 downstream gene variant G/A snv 0.59 3
rs13239597 0.882 0.080 7 129055929 non coding transcript exon variant C/A snv 9.0E-02 3
rs2227513 1.000 0.080 12 68253559 intron variant T/C snv 0.15 3
rs2280381 0.882 0.080 16 85985027 intron variant C/T snv 0.64 3
rs2732552 0.925 0.080 11 35063045 regulatory region variant T/C snv 0.51 3
rs428073 1.000 0.080 12 118244946 missense variant C/G;T snv 0.72 3
rs6914831 1.000 0.080 6 135318506 3 prime UTR variant C/T snv 0.59 0.59 3
rs6932056 0.925 0.080 6 137921300 intergenic variant T/C snv 3.4E-02 3
rs77583790 0.882 0.080 3 159976265 intron variant G/A;C snv 3
rs7897633 1.000 0.080 10 51197961 intron variant C/A snv 0.64 3
rs9373839 0.882 0.080 6 106207742 intron variant T/C snv 0.15 3
rs10245867 0.925 0.080 7 28102567 intron variant G/T snv 0.37 2
rs1028488 1.000 0.080 6 170281387 upstream gene variant G/T snv 0.46 2
rs10498070 0.925 0.080 2 219833404 intergenic variant A/C snv 0.39 2
rs10499197 0.925 0.080 6 137811379 intergenic variant T/G snv 2.4E-02 2
rs10865035 1.000 0.080 2 100219272 intron variant A/G snv 0.42 2
rs1133906 0.925 0.080 7 93135669 synonymous variant C/T snv 0.22 0.28 2
rs11755393 1.000 0.080 6 34856859 missense variant A/G;T snv 0.36 2
rs121909581 0.925 0.080 1 22639291 stop gained C/T snv 3.6E-05 2
rs14024 0.925 0.080 12 52675230 missense variant T/C snv 0.31 0.24 2
rs140490 1.000 0.080 22 21567397 intron variant G/A;C;T snv 2