Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs121909224
PTEN
0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 35
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 1
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 13
rs587781991
TP53
0.724 0.240 17 7675208 missense variant C/A;T snv 14
rs1057519978
TP53
0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs1057519977
TP53
0.763 0.360 17 7675189 missense variant G/C snv 13
rs138729528
TP53
0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 16
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 17
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
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
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
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519999
TP53
0.763 0.160 17 7674247 missense variant T/C;G snv 12
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