Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 1
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 1
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 1
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 1
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 1
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 1
rs138729528
TP53
0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 1
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 1
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 1
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 1
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 1
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 2
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 1
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 1
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 1
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 1
rs28934573
TP53
0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 1
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 1
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 1
rs121912656
TP53
0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 1
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 1
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 1
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 1
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 1
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 1