Source: BEFREE

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-06 484
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 23
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 14
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 11
rs1225976306
BRAF ; LOC105375536
0.807 0.160 7 140924673 missense variant C/T snv 9.3E-06 8
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 7
rs121913378
BRAF
0.776 0.280 7 140753337 missense variant C/A;G;T snv 6
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 5
rs3748093
BRAF
0.925 0.120 7 140800651 intron variant T/A snv 1.5E-02 4
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 4
rs114729114
BRAF
0.925 0.080 7 140910797 intron variant C/T snv 1.1E-02 3
rs121913375
BRAF
0.851 0.240 7 140753339 missense variant G/A;C snv 3
rs397507482
BRAF
0.882 0.040 7 140753386 missense variant A/C snv 3
rs868021367
BRAF
0.882 0.080 7 140753319 missense variant C/G snv 3
rs1238788540
BRAF
0.925 0.080 7 140800368 missense variant G/C snv 4.0E-06 7.0E-06 2
rs756706958
BRAF
0.925 0.080 7 140776967 missense variant T/C snv 2
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 2
rs121913371
BRAF
1.000 0.040 7 140781678 missense variant G/A;T snv 4.0E-06; 8.0E-06 2
rs730880413
BRAF
0.925 0.080 7 140801460 missense variant C/T snv 4.0E-06 2
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 2
rs121913368
BRAF
0.925 0.040 7 140753345 missense variant AG/GA mnv 2
rs1057519720
BRAF
0.851 0.080 7 140781602 missense variant CC/AA;GA mnv 2
rs775040765
BRAF
1.000 7 140800366 missense variant T/C snv 8.0E-05 1.4E-05 2