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
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
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs121913369
BRAF
0.790 0.280 7 140753346 missense variant G/A;C snv 4.0E-06 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
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 10
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs727502902
BRAF
0.882 0.080 7 140753338 inframe insertion -/TAG delins 4.0E-06 4
rs121913353
BRAF
0.925 0.160 7 140781612 missense variant C/G;T snv 3
rs397516890
BRAF
1.000 0.080 7 140781601 inframe deletion TCC/- del 1
rs397516897
BRAF
1.000 0.080 7 140753334 inframe deletion TCA/- del 1