Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs12951053
TP53
0.732 0.160 17 7674089 intron variant A/C snv 0.10 14
rs7763881
HULC ; LOC100506207
0.776 0.160 6 8653014 non coding transcript exon variant A/C snv 0.44 11
rs1057519987
TP53
0.776 0.280 17 7673810 missense variant A/C snv 10
rs7248488
ZNF208
0.851 0.160 19 22005907 intron variant A/C snv 0.59 5
rs8103163
ZNF208
0.882 0.120 19 21991950 intron variant A/C snv 0.59 4
rs10437048
PADI4
1.000 0.080 1 17356224 intron variant A/C snv 1
rs1131691021
TP53
0.716 0.120 17 7675097 missense variant A/C;G snv 21
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057519986
TP53
0.776 0.240 17 7673811 missense variant A/C;G snv 10
rs387906678
FGFR2
0.851 0.120 10 121515263 missense variant A/C;G snv 5
rs750664148
CASC11 ; MYC
0.851 0.200 8 127738434 missense variant A/C;G snv 5
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17
rs765848205
TP53
0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs1057519988
TP53
0.776 0.240 17 7673812 missense variant A/C;G;T snv 10