Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 21
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs16901979 0.724 0.480 8 127112671 intron variant C/A snv 0.16 16
rs1760944 0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 45
rs1800624 0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs767649 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs17577 0.649 0.520 20 46014472 missense variant G/A;C snv 0.16 30
rs2250889 0.667 0.520 20 46013767 missense variant G/C;T snv 0.88; 1.6E-05 23
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
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 62
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 55
rs3834129 0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 38
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 46
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs121913530 0.583 0.640 12 25245351 missense variant C/A;G;T snv 55