Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 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
rs55819519
TP53
0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 40
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 36
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 28
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 25
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 23
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 22
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 21
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 21
rs11540652
TP53
0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 20
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 20
rs121912654
TP53
0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 19
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 16
rs1800372
TP53
0.752 0.240 17 7674892 synonymous variant T/A;C snv 1.3E-02 15
rs1800371
TP53
0.742 0.240 17 7676230 missense variant G/A;T snv 1.2E-03 15
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 14
rs12951053
TP53
0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 13