Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs138729528
TP53
0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 25
rs121912657
TP53
0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 24
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 24
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 24
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 24
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 23
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 23
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 22
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 22
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 22
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 21
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs121912654
TP53
0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 21
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21