Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs55832599
TP53
0.716 0.360 17 7673821 missense variant G/A snv 5
rs764146326
TP53
0.662 0.480 17 7673779 missense variant C/A;G;T snv 4.0E-06 5
rs779196500
TP53
0.882 0.120 17 7675187 missense variant G/A snv 4.0E-06 5
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 5
rs1057520005
TP53
0.742 0.360 17 7673800 missense variant C/A;G snv 4
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 4
rs1064793929
TP53
0.882 0.280 17 7675167 frameshift variant A/-;AA delins 4
rs28934574
TP53
0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 4
rs587780071
TP53
0.732 0.240 17 7674951 missense variant G/A snv 4
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
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 3
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 2
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 2
rs1057520006
TP53
0.752 0.240 17 7673799 missense variant A/C;G;T snv 2
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 2
rs876658468
TP53
0.689 0.440 17 7674954 missense variant G/A;C;T snv 2
rs1057519982
TP53
1.000 0.080 17 7674239 missense variant A/C;G;T snv 1
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 1
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 1
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 1
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 1