Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 43
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 8
rs104894228
LRRC56 ; HRAS
0.605 0.560 11 534286 missense variant C/A;G;T snv 22
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 23
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 42
rs1056892
CBR3-AS1 ; CBR3
0.882 0.160 21 36146408 missense variant G/A snv 0.37 0.39 6
rs1057519715
ESR1
1.000 0.080 6 152098779 missense variant T/A snv 1
rs1057519738
MIR4728 ; ERBB2
0.790 0.160 17 39725079 missense variant G/A snv 4.0E-06 3
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 6
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 6
rs1057519825
BTK
0.882 0.120 X 101356176 missense variant C/G snv 6
rs1057519826
BTK
0.882 0.120 X 101356177 missense variant A/T snv 6
rs1057519827
ESR1
6 152011697 missense variant G/C snv 1
rs1057519854
FGFR2
0.882 0.080 10 121488063 missense variant A/T snv 2
rs1057519857
ERBB2 ; MIR4728
0.882 0.080 17 39724772 missense variant T/C snv 3
rs1057519890
ERBB2
0.807 0.200 17 39723966 missense variant T/A snv 1
rs1057519891
ERBB3
0.851 0.160 12 56088557 missense variant G/A;T snv 4.0E-06 1
rs1057519895
FBXW7
0.724 0.240 4 152328232 missense variant C/A;G;T snv 2
rs1057519912
MED12
0.776 0.200 X 71129408 missense variant C/G;T snv 6
rs1057519925
PIK3CA
0.683 0.560 3 179210291 missense variant G/A;C snv 1
rs1057519941
PIK3CA
0.776 0.240 3 179203761 missense variant T/C;G snv 1
rs1057519942
PIK3CA
0.724 0.320 3 179203760 missense variant G/A snv 1
rs1057519943
POLE
0.790 0.160 12 132676598 missense variant G/C;T snv 5
rs1057519946
PPP2R1A
0.732 0.280 19 52212729 missense variant C/G;T snv 1