Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587781858
TP53
0.742 0.360 17 7669671 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 12
rs1131691036
TP53
0.851 0.080 17 7675207 frameshift variant GCA/CC delins 8
rs587782144
TP53
0.807 0.160 17 7675139 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 8
rs587782596
TP53
0.807 0.200 17 7675071 missense variant G/A;T snv 7
rs397516435
TP53
0.851 0.280 17 7674945 stop gained G/A;C snv 4.0E-06 6
rs1288373809
TP53
0.882 0.120 17 7673255 synonymous variant G/A snv 5.3E-06 5
rs1457582183
TP53
0.827 0.200 17 7673608 missense variant G/A;C snv 7.0E-06 5
rs375275361
TP53
0.827 0.120 17 7675054 missense variant A/G;T snv 1.2E-05; 4.0E-06 5
rs779196500
TP53
0.882 0.120 17 7675187 missense variant G/A snv 4.0E-06 5
rs2287499
WRAP53 ; TP53
0.925 0.080 17 7688850 missense variant C/G;T snv 0.20 4
rs1064795369
TP53
0.882 0.080 17 7673791 missense variant A/C;G snv 3
rs1159579789
TP53
0.925 0.080 17 7673578 missense variant T/C snv 4.0E-06 3
rs372201428
TP53
0.882 0.120 17 7676181 missense variant G/A;C snv 1.2E-05 3
rs587781433
TP53
0.925 0.080 17 7674197 missense variant T/C;G snv 3
rs1064794312
TP53
0.925 0.080 17 7674278 missense variant A/G snv 8.0E-06 2
rs1177881399
TP53
0.925 0.080 17 7673557 missense variant T/C snv 4.0E-06 2
rs1237722021
TP53
0.925 0.080 17 7676194 missense variant C/A snv 7.0E-06 2
rs587782646
TP53
0.925 0.080 17 7676576 missense variant C/G snv 4.0E-06 2