Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs35407685
BRAF
1.000 0.080 7 140786444 intron variant -/G delins 1
rs727502902
BRAF
0.882 0.080 7 140753338 inframe insertion -/TAG delins 4.0E-06 4
rs397507482
BRAF
0.882 0.040 7 140753386 missense variant A/C snv 3
rs397516893
BRAF
0.925 0.160 7 140778048 missense variant A/C snv 3
rs180177033
BRAF
1.000 0.080 7 140781620 missense variant A/C snv 1
rs397507480
BRAF
1.000 0.160 7 140754233 missense variant A/C snv 1
rs397509343
BRAF
1.000 0.160 7 140801531 missense variant A/C snv 1
rs6464149
BRAF ; LOC105375536
1.000 0.080 7 140926036 upstream gene variant A/C snv 0.12 1
rs869025606
BRAF
1.000 0.160 7 140781609 missense variant A/C snv 1
rs397516903
BRAF
0.925 0.200 7 140801533 missense variant A/C;G snv 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs869025340
BRAF
0.925 0.160 7 140777032 missense variant A/C;G;T snv 5
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 12
rs180177042
BRAF
0.807 0.280 7 140749365 missense variant A/C;T snv 8
rs121913341
BRAF
0.851 0.280 7 140753350 missense variant A/C;T snv 5
rs121913337
BRAF
0.925 0.200 7 140753353 missense variant A/C;T snv 2
rs794729219
BRAF
0.882 0.240 7 140753352 missense variant A/G snv 3
rs397507475
BRAF
0.925 0.200 7 140778054 missense variant A/G snv 2
rs121913225
BRAF
1.000 0.040 7 140753351 missense variant A/G snv 1
rs397507473
BRAF
1.000 0.160 7 140781605 missense variant A/G snv 4.0E-06 1
rs11762469
BRAF
1.000 0.080 7 140914412 intron variant A/G;T snv 2
rs9648716
BRAF
1.000 0.080 7 140912363 intron variant A/G;T snv 0.31 1
rs397516895
BRAF
0.827 0.280 7 140753392 missense variant A/T snv 5
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913368
BRAF
0.925 0.040 7 140753345 missense variant AG/GA mnv 2