Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 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
rs587780071
TP53
0.732 0.240 17 7674951 missense variant G/A snv 11
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 16
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
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