Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 20
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs61764370 0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 55
rs7977932 0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs771386507 0.882 0.120 6 31355479 missense variant C/T snv 4.0E-06 6
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 484
rs2303428 0.776 0.240 2 47476361 splice region variant T/A;C;G snv 4.0E-06; 0.12 9
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 135
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 62
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47