Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691041
TP53
17 7676271 frameshift variant -/A delins 2
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 213
rs866419664
TP53
0.882 0.040 17 7673821 frameshift variant -/TCCCA delins 5
rs17880560
TP53
17 7668169 intron variant -/TGGCCG delins 2
rs764803020
TP53
0.851 0.040 17 7673750 frameshift variant -/TTTCCGCCGG delins 4.0E-06 5
rs1064793929
TP53
0.882 0.280 17 7675167 frameshift variant A/-;AA delins 4
rs12951053
TP53
0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs1453167097
TP53
0.925 0.080 17 7675172 missense variant A/C snv 2
rs989692988
TP53
17 7676023 splice donor variant A/C snv 8.0E-06 1
rs1057519987
TP53
0.776 0.280 17 7673810 missense variant A/C snv 1
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs1064795369
TP53
0.882 0.080 17 7673791 missense variant A/C;G snv 3
rs587781386
TP53
0.882 0.120 17 7674889 missense variant A/C;G snv 3.2E-05; 4.0E-06 3
rs9894946
TP53
0.925 0.160 17 7667762 intron variant A/C;G snv 2
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 21
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 16
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 6
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 5
rs587782289
TP53
0.752 0.240 17 7674257 missense variant A/C;G;T snv 3
rs1057520006
TP53
0.752 0.240 17 7673799 missense variant A/C;G;T snv 2
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 2
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 1
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 1
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 1