Gene: FCGR2A ×
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: rs1801274
rs1801274
FCGR2A
46 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.850 1.000 9 2009 2018
dbSNP: rs6671847
rs6671847
FCGR2A
2 0.925 0.120 1 161509020 intron variant G/A snv 0.43 0.710 1.000 2 2009 2015
dbSNP: rs61802846
rs61802846
FCGR2A
5 0.827 0.120 1 161504083 upstream gene variant A/C snv 8.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs511278
rs511278
FCGR2A
1 1.000 0.040 1 161521106 intron variant T/A;C snv 0.010 1.000 1 2018 2018