Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs730882008
TP53
0.683 0.440 17 7673775 missense variant C/A;G;T snv 4.0E-06 1
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 1
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 1
rs28934578
TP53
0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 36
rs121912654
TP53
0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 19
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 4
rs876660754
TP53
0.701 0.360 17 7675095 missense variant C/A;T snv 4
rs587781991
TP53
0.724 0.240 17 7675208 missense variant C/A;T snv 3
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 1
rs754332870
TP53
0.790 0.240 17 7676240 missense variant C/G snv 4.0E-06 9
rs1288373809
TP53
0.882 0.120 17 7673255 synonymous variant G/A snv 5.3E-06 5
rs55832599
TP53
0.716 0.360 17 7673821 missense variant G/A snv 5
rs779196500
TP53
0.882 0.120 17 7675187 missense variant G/A snv 4.0E-06 5
rs587780071
TP53
0.732 0.240 17 7674951 missense variant G/A snv 4
rs121912651
TP53
0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 21
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 9
rs1457582183
TP53
0.827 0.200 17 7673608 missense variant G/A;C snv 7.0E-06 5
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 5
rs28934574
TP53
0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 4
rs121913343
TP53
0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 20
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 2
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 1
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 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