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
rs1057519997
TP53
0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 17
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 16
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
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
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
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
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 19
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
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