Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12951053
TP53
0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs12947788
TP53
0.776 0.280 17 7674109 intron variant G/A snv 0.10 8
rs12602273
TP53
0.851 0.080 17 7679695 intron variant C/G snv 0.15 4
rs2078486
TP53
0.882 0.080 17 7679765 intron variant G/A;C snv 3
rs2287497
WRAP53 ; TP53
0.882 0.120 17 7689462 intron variant G/A snv 0.25 3
rs17880560
TP53
17 7668169 intron variant -/TGGCCG delins 2
rs59758982
TP53
0.925 0.040 17 7676326 intron variant TCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCC/-;TCCAGGTCCCCAGCCC;TCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCC delins 0.82 2
rs9894946
TP53
0.925 0.160 17 7667762 intron variant A/C;G snv 2
rs8079544
TP53
1.000 0.040 17 7676734 intron variant C/T snv 7.4E-02 2
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 9
rs876659384
TP53
0.851 0.240 17 7673552 stop gained C/A snv 5
rs201744589
TP53
0.882 0.240 17 7673728 stop gained C/A;G;T snv 4.0E-06; 1.2E-05 3
rs397516435
TP53
0.851 0.280 17 7674945 stop gained G/A;C snv 4.0E-06 3
rs1429743956
TP53
0.882 0.080 17 7674906 stop gained T/A;C snv 3
rs1131691026
TP53
0.925 0.160 17 7675174 stop gained C/T snv 1
rs1206165503
TP53
0.925 0.160 17 7675175 stop gained C/T snv 1
rs1057523347
TP53
0.925 0.160 17 7673789 stop gained A/G;T snv 1
rs879253911
TP53
0.925 0.200 17 7675074 stop gained C/A;T snv 1
rs730882029
TP53
0.882 0.200 17 7670685 stop gained G/A snv 1
rs1213207387
WRAP53 ; TP53
1.000 0.120 17 7689255 stop gained C/G;T snv 4.0E-06 1
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 1
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 56
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47