Source: CLINVAR ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397514698
GNAQ
0.667 0.400 9 77797577 missense variant C/T snv 41
rs387906760
STAT1
0.790 0.200 2 190995184 missense variant C/T snv 12
rs797044484
TP63
0.776 0.400 3 189868624 missense variant C/G snv 10