Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519978
TP53
0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 42
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 39
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 20
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs121912657
TP53
0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 15
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 21
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs786201419
TP53
0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37
rs28934574
TP53
0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27