Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519999
TP53
0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519947
PPP2R1A
0.790 0.160 19 52212730 missense variant G/A snv 9
rs786201419
TP53
0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs587782177
TP53
0.763 0.200 17 7674887 missense variant C/A;G;T snv 11
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 10
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs587781991
TP53
0.724 0.240 17 7675208 missense variant C/A;T snv 14
rs867384286
FBXW7
0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
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
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs1057520004
TP53
0.752 0.240 17 7674884 missense variant A/C;T snv 11
rs587780071
TP53
0.732 0.240 17 7674951 missense variant G/A snv 11
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
rs786203071
TP53
0.776 0.240 17 7675181 missense variant T/A;G snv 8
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057519946
PPP2R1A
0.732 0.280 19 52212729 missense variant C/G;T snv 17
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 16