Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918094
TTR
0.827 0.280 18 31592921 missense variant T/C snv 1
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 1
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 1
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 1
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 1
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 1
rs121912656
TP53
0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 1
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 1
rs138729528
TP53
0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 1
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 1
rs28934574
TP53
0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 1
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 1
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 1
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 1
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 1
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 1
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 1
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 1
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 1
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 1
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 1
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 1
rs786203071
TP53
0.776 0.240 17 7675181 missense variant T/A;G snv 1
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 1