Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 11
rs1057519997
TP53
0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 19
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 18
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 16
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 15
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057520005
TP53
0.742 0.360 17 7673800 missense variant C/A;G snv 11
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 25
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 17
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 13
rs28934574
TP53
0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 27
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 23
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 22
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 22
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 19