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: rs672601308
rs672601308
USP8
1 1.000 0.080 15 50490444 missense variant C/G snv 0.800 1.000 1 2017 2017