Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
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
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
rs17849781
TP53
0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs1057519977
TP53
0.763 0.360 17 7675189 missense variant G/C snv 13
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
rs1057519999
TP53
0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs786201419
TP53
0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs786203071
TP53
0.776 0.240 17 7675181 missense variant T/A;G snv 8