Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691023
TP53
1.000 0.080 17 7675142 missense variant A/G;T snv 2
rs751477326
TP53
1.000 0.080 17 7675082 missense variant G/A;C snv 4.0E-06 3
rs121912667
TP53
0.851 0.200 17 7673766 missense variant T/A snv 4
rs375338359
TP53
0.882 0.200 17 7670684 missense variant C/G;T snv 8.0E-06 4
rs730882029
TP53
0.882 0.200 17 7670685 stop gained G/A snv 4
rs1060501205
TP53
0.827 0.120 17 7673749 missense variant TG/GT mnv 5
rs587782529
TP53
0.851 0.200 17 7670700 missense variant G/A;C snv 8
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs587781991
TP53
0.724 0.240 17 7675208 missense variant C/A;T snv 17
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs866775781
TP53
0.716 0.440 17 7675216 splice acceptor variant C/A;G snv 17
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 19
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 19
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G 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
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 21
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs786201057
TP53
0.677 0.400 17 7675995 missense variant G/A;C;T snv 24
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 34
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47