Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7705526 0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 11
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 11
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 10
rs56113850 0.807 0.080 19 40847202 intron variant T/C snv 0.52 8
rs55781567 0.851 0.080 15 78565644 5 prime UTR variant C/G snv 0.31 7
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 6
rs1800440 0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 6
rs2853677 0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 6
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 5
rs8040868 0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 5
rs1470579 0.925 0.160 3 185811292 intron variant A/C snv 0.46 4
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 4
rs3117582 0.716 0.440 6 31652743 intron variant T/G snv 7.1E-02 3
rs667282 0.790 0.120 15 78571130 intron variant T/C snv 0.28 3
rs31490 0.776 0.280 5 1344343 splice region variant G/A;T snv 0.37; 8.0E-06 3
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs7741164 0.882 0.080 6 41525674 intron variant G/A snv 6.6E-02 3
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 3
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 3
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 3
rs11375254 0.882 0.080 3 189625454 intergenic variant A/-;AA;AAA;AAAA delins 3
rs7086803 0.763 0.160 10 112738717 intron variant G/A snv 0.20 3