Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs7867494 0.882 0.120 9 74529284 intron variant A/G snv 0.27 6
rs8100239 0.882 0.200 19 44749847 intron variant T/A snv 0.38 5
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs3212986 0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs10012 0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1050171 0.851 0.120 7 55181370 missense variant G/A;C snv 0.52; 4.0E-06 6
rs1051266 0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs1057519788 0.925 0.080 6 117317184 missense variant C/T snv 6
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
rs1057519861 0.776 0.080 7 55181398 missense variant T/A snv 15
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70