Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913226
BRAF
1.000 0.040 7 140753332 inframe deletion TTT/- del 1
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv 10
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913378
BRAF
0.776 0.280 7 140753337 missense variant C/A;G;T snv 11
rs121913375
BRAF
0.851 0.240 7 140753339 missense variant G/A;C snv 7
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 12
rs121913368
BRAF
0.925 0.040 7 140753345 missense variant AG/GA mnv 2
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 12
rs121913361
BRAF
0.807 0.280 7 140753349 missense variant C/A;G;T snv 7
rs121913341
BRAF
0.851 0.280 7 140753350 missense variant A/C;T snv 5
rs121913225
BRAF
1.000 0.040 7 140753351 missense variant A/G snv 1
rs794729219
BRAF
0.882 0.240 7 140753352 missense variant A/G snv 3
rs121913337
BRAF
0.925 0.200 7 140753353 missense variant A/C;T snv 2
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs1057519718
BRAF
0.925 0.160 7 140753355 missense variant CA/TC mnv 2
rs121913363
BRAF
1.000 0.040 7 140753361 missense variant T/C snv 1
rs397507482
BRAF
0.882 0.040 7 140753386 missense variant A/C snv 3
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 10
rs1639679
BRAF
1.000 0.040 7 140778454 intron variant G/T snv 9.8E-02 1
rs121913376
BRAF
0.925 0.080 7 140781597 missense variant C/A;T snv 2
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42