Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1000256867
TP53
17 7673550 missense variant T/A;G snv 4.0E-06 1
rs1011445550
TP53
0.925 0.080 17 7676391 missense variant G/C snv 2
rs1019340046
TP53
0.882 0.080 17 7674225 missense variant C/T snv 5
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1057517840
TP53
0.925 0.200 17 7674904 frameshift variant CT/- delins 3
rs1057517983
TP53
1.000 0.120 17 7674232 missense variant C/A;G;T snv 1
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1057519976
TP53
17 7675207 missense variant G/A;C snv 1
rs1057519977
TP53
0.763 0.360 17 7675189 missense variant G/C snv 13
rs1057519978
TP53
0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs1057519980
TP53
1.000 17 7675084 missense variant G/C snv 1
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs1057519982
TP53
1.000 0.080 17 7674239 missense variant A/C;G;T snv 1
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs1057519984
TP53
0.882 0.080 17 7673777 missense variant G/C;T snv 3
rs1057519985
TP53
0.724 0.360 17 7673763 missense variant T/A;C;G snv 16
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
rs1057519988
TP53
0.776 0.240 17 7673812 missense variant A/C;G;T snv 10
rs1057519989
TP53
0.732 0.240 17 7674233 missense variant C/A;G;T snv 17
rs1057519991
TP53
0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26
rs1057519992
TP53
0.742 0.400 17 7674890 missense variant T/A;C;G snv 14
rs1057519995
TP53
0.807 0.240 17 7674200 missense variant T/A snv 9
rs1057519996
TP53
0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 19