Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800371
TP53
0.742 0.240 17 7676230 missense variant G/A;T snv 1.2E-03 15
rs1800372
TP53
0.752 0.240 17 7674892 synonymous variant T/A;C snv 1.3E-02 15
rs375874539
TP53
0.732 0.320 17 7674237 missense variant G/A;C snv 15
rs587780071
TP53
0.732 0.240 17 7674951 missense variant G/A snv 15
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 15
rs587782664
TP53
0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 15
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 15
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 14
rs1057520005
TP53
0.742 0.360 17 7673800 missense variant C/A;G snv 14
rs1057520006
TP53
0.752 0.240 17 7673799 missense variant A/C;G;T snv 14
rs12951053
TP53
0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs1057519977
TP53
0.763 0.360 17 7675189 missense variant G/C snv 13
rs1625895
TP53
0.752 0.200 17 7674797 non coding transcript exon variant T/A;C;G snv 9.1E-06; 0.86; 4.5E-06 13
rs876660333
TP53
0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519978
TP53
0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs1057519999
TP53
0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs1057520004
TP53
0.752 0.240 17 7674884 missense variant A/C;T snv 12
rs1131691003
TP53
0.752 0.360 17 7676381 splice donor variant C/A;G snv 12
rs1131691042
TP53
0.752 0.360 17 7675052 splice donor variant C/T snv 12
rs587781858
TP53
0.742 0.360 17 7669671 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 12
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs876660807
TP53
0.763 0.160 17 7674248 missense variant T/C snv 12
rs587782177
TP53
0.763 0.200 17 7674887 missense variant C/A;G;T snv 11
rs1057519986
TP53
0.776 0.240 17 7673811 missense variant A/C;G snv 10
rs1057519987
TP53
0.776 0.280 17 7673810 missense variant A/C snv 10