Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519949
RHEB
0.851 0.120 7 151490964 missense variant A/T snv 4
rs1057519950
RHEB
0.827 0.200 7 151490963 missense variant T/A;C snv 4
rs1057519786
ARAF
0.882 0.160 X 47566722 missense variant C/G;T snv 3
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