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: rs10127939
rs10127939
FCGR3A
5 0.851 0.160 1 161548543 missense variant A/C;T snv 4.3E-02; 5.5E-02 0.010 1.000 1 2012 2012
dbSNP: rs387906758
rs387906758
STAT1
6 0.851 0.080 2 190995185 missense variant G/A;C snv 0.010 1.000 1 2019 2019
dbSNP: rs761007181
rs761007181
FCGR3B
1 1 161629900 missense variant A/C;T snv 0.010 1.000 1 2012 2012