Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 9
rs180177040
BRAF
0.790 0.360 7 140754187 missense variant T/C;G snv 9
rs121913470
ERBB2
0.776 0.200 17 39723967 missense variant T/C;G snv 7
rs1057519876
ARAF
0.882 0.160 X 47566721 missense variant T/G snv 3
rs121913469
ERBB2
0.763 0.240 17 39723966 missense variant TT/CC mnv 8