Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913469
ERBB2
0.763 0.240 17 39723966 missense variant TT/CC mnv 1
rs28933368
ERBB2 ; MIR4728
0.851 0.080 17 39725721 missense variant G/A snv 1
rs28933369
MIR4728 ; ERBB2
0.925 0.080 17 39724744 missense variant G/A snv 1
rs28933370
MIR4728 ; ERBB2
0.882 0.120 17 39725125 missense variant A/G snv 7.0E-06 1