Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1801195
WRN
0.776 0.240 8 31141764 missense variant G/A;T snv 8.0E-06; 0.45 0.46 8
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs20551 0.752 0.320 22 41152004 missense variant A/G snv 0.31 0.23 10
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs2234922 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs12917 0.605 0.480 10 129708019 missense variant C/T snv 0.14 0.14 45
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs35090414 0.925 0.120 11 45224227 missense variant G/A;T snv 1.5E-04; 8.2E-02 2
rs2070770 0.925 0.120 11 60463058 synonymous variant C/T snv 7.1E-02 5.4E-02 2
rs111724149 0.925 0.120 11 45204720 missense variant A/G snv 1.8E-03 1.8E-03 2
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs770027749 0.925 0.120 22 28795623 missense variant C/A;G snv 8.0E-06 2
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs1057520009 0.790 0.200 2 61492337 missense variant C/T snv 4.4E-06 14
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs1390458638 0.925 0.120 2 219216441 missense variant G/A snv 4.0E-06 2
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 27
rs1227230819 0.925 0.120 5 37815877 missense variant T/C snv 4.0E-06 2
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 35
rs1057519834 0.658 0.480 1 114713908 missense variant TG/CT mnv 31