Gene: FGA ×
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: rs2070016
rs2070016
FGA
4 1.000 0.040 4 154589162 intron variant A/G snv 0.12 0.700 1.000 1 2011 2011
dbSNP: rs6050
rs6050
FGA
10 0.827 0.120 4 154586438 missense variant T/A;C snv 0.29 0.700 1.000 1 2011 2011