Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs786202962
TP53
0.701 0.320 17 7675085 missense variant C/A;T snv 4.0E-06 21
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057520003
TP53
0.695 0.320 17 7675996 missense variant T/G snv 20
rs730882005
TP53
0.701 0.400 17 7674250 missense variant C/A;G;T snv 8.0E-06 20
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 20
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T 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
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
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs942158624
TP53
0.724 0.320 17 7674948 missense variant T/A snv 19
rs55832599
TP53
0.716 0.360 17 7673821 missense variant G/A snv 18
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 17
rs148924904
TP53
0.724 0.360 17 7675124 missense variant T/C snv 7.0E-06 17
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
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 16
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 16
rs876659802
TP53
0.732 0.440 17 7673787 missense variant G/A;C;T snv 16
rs985033810
TP53
0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 15