Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs786204847
rs786204847
DDX58
2 1.000 9 32488039 missense variant T/G snv 0.800 0
dbSNP: rs786204848
rs786204848
DDX58
4 0.882 0.040 9 32488884 missense variant C/A snv 0.800 0