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
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs28934576
TP53
0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 47
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
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 23
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 21
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 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
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 14
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 13
rs121912656
TP53
0.662 0.560 17 7674229 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 11
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 9
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 9
rs754332870
TP53
0.790 0.240 17 7676240 missense variant C/G snv 4.0E-06 9
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 8
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 7
rs587782329
TP53
0.677 0.280 17 7674217 missense variant C/A;G;T snv 7
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 6
rs1288373809
TP53
0.882 0.120 17 7673255 synonymous variant G/A snv 5.3E-06 5