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: rs121913094
rs121913094
FGG
1 1.000 0.080 4 154606767 missense variant T/A snv 0.700 1.000 4 1986 2005