Source: CLINVAR ×
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 1
rs1057519987
TP53
0.776 0.280 17 7673810 missense variant A/C snv 9
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
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 21
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 20
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 18
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
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 16
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 15
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 13
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
rs1057519997
TP53
0.776 0.320 17 7676037 missense variant A/C;G;T snv 9
rs876659675
TP53
0.807 0.280 17 7674199 missense variant A/C;G;T snv 7
rs1057520004
TP53
0.752 0.240 17 7674884 missense variant A/C;T snv 11
rs2273535
AURKA
0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 1
rs1057519983
TP53
0.724 0.360 17 7673797 missense variant A/G snv 16
rs121913474
FGFR2
0.790 0.200 10 121515260 missense variant A/G snv 3
rs879253942
TP53
0.677 0.400 17 7673826 missense variant A/G snv 3