Gene: FGG ×
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: rs148685782
rs148685782
FGG
4 1.000 0.080 4 154611883 missense variant G/C snv 1.9E-03 2.2E-03 0.700 1.000 1 2016 2016
dbSNP: rs2066861
rs2066861
FGG
5 4 154606284 intron variant C/T snv 0.26 0.700 1.000 1 2011 2011