Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 4
rs121913341
BRAF
0.851 0.280 7 140753350 missense variant A/C;T snv 2
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 2
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 2
rs387906661
BRAF
0.807 0.280 7 140801551 missense variant T/G snv 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 1
rs180177032
BRAF
1.000 0.080 7 140781623 missense variant C/A snv 1
rs180177033
BRAF
1.000 0.080 7 140781620 missense variant A/C snv 1
rs121913348
BRAF
0.763 0.480 7 140781617 missense variant C/A;G;T snv 1
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 1
rs121913340
BRAF
1.000 0.120 7 140753379 missense variant C/T snv 1
rs121913375
BRAF
0.851 0.240 7 140753339 missense variant G/A;C snv 1
rs869025606
BRAF
1.000 0.160 7 140781609 missense variant A/C snv 1
rs397507466
BRAF
0.807 0.280 7 140801537 missense variant T/A;C;G snv 4.0E-06 1
rs397507483
BRAF
0.790 0.400 7 140753348 missense variant C/A;T snv 1
rs397507486
BRAF
1.000 0.160 7 140739813 missense variant T/C snv 1
rs869025340
BRAF
0.925 0.160 7 140777032 missense variant A/C;G;T snv 1
rs180177034
BRAF
0.882 0.200 7 140801536 missense variant C/G snv 1
rs180177035
BRAF
0.752 0.280 7 140801502 missense variant T/C snv 1
rs397507476
BRAF
0.882 0.200 7 140778011 missense variant T/A;G snv 1
rs397507470
BRAF
1.000 0.160 7 140801488 missense variant G/T snv 1
rs397507473
BRAF
1.000 0.160 7 140781605 missense variant A/G snv 4.0E-06 1
rs180177040
BRAF
0.790 0.360 7 140754187 missense variant T/C;G snv 1
rs180177042
BRAF
0.807 0.280 7 140749365 missense variant A/C;T snv 1
rs180177036
BRAF
0.925 0.200 7 140778053 missense variant C/A;G snv 1