Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 32
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 16
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 12
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 11
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv 10
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 9
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 8
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 8
rs121913361
BRAF
0.807 0.280 7 140753349 missense variant C/A;G;T snv 6
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 6
rs121913378
BRAF
0.776 0.280 7 140753337 missense variant C/A;G;T snv 6
rs121913375
BRAF
0.851 0.240 7 140753339 missense variant G/A;C snv 5
rs121913341
BRAF
0.851 0.280 7 140753350 missense variant A/C;T snv 3
rs1057519720
BRAF
0.851 0.080 7 140781602 missense variant CC/AA;GA mnv 2
rs121913337
BRAF
0.925 0.200 7 140753353 missense variant A/C;T snv 2
rs121913349
BRAF
0.925 0.200 7 140781618 missense variant C/G;T snv 2
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs794729219
BRAF
0.882 0.240 7 140753352 missense variant A/G snv 2
rs1057519718
BRAF
0.925 0.160 7 140753355 missense variant CA/TC mnv 1
rs121913225
BRAF
1.000 0.040 7 140753351 missense variant A/G snv 1
rs121913226
BRAF
1.000 0.040 7 140753332 inframe deletion TTT/- del 1