Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs483352697
TP53
0.695 0.480 17 7674944 missense variant C/A;G;T snv 4.0E-06 17
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 17
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 13
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 10
rs587782177
TP53
0.763 0.200 17 7674887 missense variant C/A;G;T snv 11
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 14
rs1057520004
TP53
0.752 0.240 17 7674884 missense variant A/C;T snv 11
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 12
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 12
rs765848205
TP53
0.763 0.240 17 7674253 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
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs28934573
TP53
0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 24
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs121912656
TP53
0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 20
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 37