Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1060501205
TP53
0.827 0.120 17 7673749 missense variant TG/GT mnv 5
rs59758982
TP53
0.925 0.040 17 7676326 intron variant TCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCC/-;TCCAGGTCCCCAGCCC;TCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCCTCCAGGTCCCCAGCCC delins 0.82 2
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 22
rs764562217
TP53
0.882 0.120 17 7673308 stop lost T/G snv 2.3E-05 3.5E-05 3
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 23
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 13
rs1060501201
TP53
0.925 0.080 17 7674190 missense variant T/C;G snv 4
rs747342068
TP53
0.695 0.440 17 7675218 missense variant T/C;G snv 4.0E-06 4
rs1060501198
TP53
0.925 0.040 17 7674900 missense variant T/C;G snv 3
rs587781433
TP53
0.925 0.080 17 7674197 missense variant T/C;G snv 2
rs730882026
TP53
0.742 0.440 17 7674256 missense variant T/C;G snv 2
rs587780073
TP53
0.708 0.400 17 7674262 missense variant T/C;G snv 2
rs587782447
TP53
1.000 0.080 17 7676049 missense variant T/C;G snv 1
rs730882002
TP53
0.925 0.040 17 7674956 missense variant T/C snv 6
rs867114783
TP53
17 7675109 missense variant T/C snv 5
rs781490101
TP53
0.851 0.040 17 7673748 missense variant T/C snv 8.0E-06 5
rs1159579789
TP53
0.925 0.080 17 7673578 missense variant T/C snv 4.0E-06 3
rs1555525126
TP53
0.925 0.120 17 7673749 missense variant T/C snv 3
rs876659477
TP53
0.882 0.040 17 7673730 missense variant T/C snv 3
rs1177881399
TP53
0.925 0.080 17 7673557 missense variant T/C snv 4.0E-06 2
rs1460793472
TP53
17 7676187 missense variant T/C snv 4.0E-06 1
rs746601313
TP53
17 7674203 missense variant T/C snv 1.6E-05 7.0E-06 1
rs879254249
TP53
1.000 0.120 17 7675122 missense variant T/C snv 1
rs141402957
TP53
1.000 0.040 17 7670658 missense variant T/C snv 1
rs72661120
TP53
17 7673717 synonymous variant T/C snv 2.7E-04 7.0E-05 1