Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs786201419
TP53
0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs1057519986
TP53
0.776 0.240 17 7673811 missense variant A/C;G snv 10
rs1057519988
TP53
0.776 0.240 17 7673812 missense variant A/C;G;T snv 10
rs1057519987
TP53
0.776 0.280 17 7673810 missense variant A/C snv 9
rs1057519997
TP53
0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs786203071
TP53
0.776 0.240 17 7675181 missense variant T/A;G snv 8
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
rs587782177
TP53
0.763 0.200 17 7674887 missense variant C/A;G;T snv 11
rs1057520006
TP53
0.752 0.240 17 7673799 missense variant A/C;G;T snv 12
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 13
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 12
rs1057520005
TP53
0.742 0.360 17 7673800 missense variant C/A;G snv 11
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 11
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 15
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs587781991
TP53
0.724 0.240 17 7675208 missense variant C/A;T snv 14