Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs180177035
BRAF
0.752 0.280 7 140801502 missense variant T/C snv 35
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 20
rs397507483
BRAF
0.790 0.400 7 140753348 missense variant C/A;T snv 13
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 12
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 12
rs180177039
BRAF
0.851 0.160 7 140778006 missense variant T/A;C;G snv 12
rs397507478
BRAF
0.790 0.440 7 140777014 missense variant C/A snv 12
rs121913378
BRAF
0.776 0.280 7 140753337 missense variant C/A;G;T snv 11
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 10
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 10
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
rs180177040
BRAF
0.790 0.360 7 140754187 missense variant T/C;G snv 9
rs180177042
BRAF
0.807 0.280 7 140749365 missense variant A/C;T snv 8
rs1225976306
BRAF ; LOC105375536
0.807 0.160 7 140924673 missense variant C/T snv 9.3E-06 8
rs121913361
BRAF
0.807 0.280 7 140753349 missense variant C/A;G;T snv 7
rs121913375
BRAF
0.851 0.240 7 140753339 missense variant G/A;C snv 7