Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913353
BRAF
0.925 0.160 7 140781612 missense variant C/G;T snv 1
rs80357468
BRCA1
0.882 0.200 17 43094415 stop gained C/T snv 1
rs75316749
LOC107986051
0.701 0.280 3 169043635 intergenic variant A/G snv 4.2E-02 1
rs587776650
NBN
0.790 0.280 8 89971214 frameshift variant GTTTT/- delins 2.0E-04 1
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
rs121913272
PIK3CA
0.752 0.400 3 179210192 missense variant T/C;G snv 1
rs121913286
PIK3CA
0.677 0.280 3 179218306 missense variant C/A;G snv 1
rs397517201
PIK3CA
0.732 0.240 3 179218307 missense variant A/C;G;T snv 1
rs121909229
PTEN
0.683 0.400 10 87933148 missense variant G/A;C;T snv 1
rs398123316
PTEN
0.851 0.160 10 87925530 missense variant A/G;T snv 1
rs587782360
PTEN
0.851 0.280 10 87933162 missense variant A/G snv 1
rs1057519995
TP53
0.807 0.240 17 7674200 missense variant T/A snv 1
rs11540654
TP53
0.925 0.200 17 7676040 missense variant C/A;G;T snv 4.8E-05 1
rs1206165503
TP53
0.925 0.160 17 7675175 stop gained C/T snv 1
rs121912655
TP53
0.724 0.400 17 7674238 missense variant C/A;G;T snv 1
rs193920774
TP53
0.695 0.440 17 7673823 missense variant C/A;T snv 1
rs28934874
TP53
0.695 0.480 17 7675161 missense variant G/A;C;T snv 1
rs483352695
TP53
0.882 0.200 17 7674227 missense variant T/A;C;G snv 1
rs587780070
TP53
0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 1
rs587781288
TP53
0.732 0.440 17 7675190 missense variant C/A;T snv 1
rs730882029
TP53
0.882 0.200 17 7670685 stop gained G/A snv 1
rs786201059
TP53
0.701 0.360 17 7673764 stop gained C/A;G;T snv 1
rs786201838
TP53
0.683 0.440 17 7674953 missense variant T/A;C;G snv 1
rs863224451
TP53
0.701 0.440 17 7673796 missense variant C/A;G;T snv 1