Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507478
BRAF
0.790 0.440 7 140777014 missense variant C/A snv 12
rs180177032
BRAF
1.000 0.080 7 140781623 missense variant C/A snv 1
rs180177036
BRAF
0.925 0.200 7 140778053 missense variant C/A;G snv 2
rs606231228
BRAF
0.925 0.160 7 140777013 missense variant C/A;G snv 2
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 20
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs121913378
BRAF
0.776 0.280 7 140753337 missense variant C/A;G;T snv 11
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs121913361
BRAF
0.807 0.280 7 140753349 missense variant C/A;G;T snv 7
rs397507483
BRAF
0.790 0.400 7 140753348 missense variant C/A;T snv 13
rs121913376
BRAF
0.925 0.080 7 140781597 missense variant C/A;T snv 2
rs180177041
BRAF
0.851 0.240 7 140777006 missense variant C/G snv 5
rs180177034
BRAF
0.882 0.200 7 140801536 missense variant C/G snv 3
rs868021367
BRAF
0.882 0.080 7 140753319 missense variant C/G snv 3
rs397516905
BRAF
1.000 0.160 7 140801479 missense variant C/G snv 1
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs180177038
BRAF
0.851 0.200 7 140778007 missense variant C/G;T snv 4
rs121913353
BRAF
0.925 0.160 7 140781612 missense variant C/G;T snv 3
rs121913349
BRAF
0.925 0.200 7 140781618 missense variant C/G;T snv 2
rs1325951163
BRAF
1.000 7 140801517 missense variant C/G;T snv 4.0E-06 1
rs1225976306
BRAF ; LOC105375536
0.807 0.160 7 140924673 missense variant C/T snv 9.3E-06 8
rs114729114
BRAF
0.925 0.080 7 140910797 intron variant C/T snv 1.1E-02 3
rs730880413
BRAF
0.925 0.080 7 140801460 missense variant C/T snv 4.0E-06 2
rs121913340
BRAF
1.000 0.120 7 140753379 missense variant C/T snv 1