Gene: FGB ×
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: rs1800790
rs1800790
FGB
9 0.851 0.200 4 154562556 upstream gene variant G/A snv 0.15 0.010 1.000 1 2016 2016
dbSNP: rs750593479
rs750593479
FGB
2 1.000 0.080 4 154565881 missense variant C/T snv 8.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs771406104
rs771406104
FGB
2 1.000 0.080 4 154569191 missense variant T/C snv 4.0E-06 0.010 1.000 1 2016 2016