Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs121909231
PTEN
0.667 0.600 10 87961095 stop gained C/A;T snv 32
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 28
rs180177135
PALB2
0.716 0.520 16 23607891 frameshift variant T/- del 2.1E-05 27
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs121909219
PTEN
0.689 0.400 10 87957915 stop gained C/A;T snv 25
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 24
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 24
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 23
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 22
rs587781525
TP53
0.689 0.480 17 7673778 missense variant T/A;C;G snv 22
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 21
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 20
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 20
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 20
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 19
rs121913293
PTEN
0.732 0.360 10 87952142 missense variant C/A;T snv 18