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: rs150830931
rs150830931
FECH
2 0.925 0.160 18 57580082 missense variant G/A;C snv 2.8E-05; 9.3E-04 0.020 1.000 2 2002 2006
dbSNP: rs118204039
rs118204039
FECH
2 0.925 0.160 18 57550734 missense variant A/G snv 0.010 1.000 1 1992 1992
dbSNP: rs150146721
rs150146721
FECH
2 0.925 0.160 18 57554336 missense variant G/A snv 4.8E-05 6.3E-05 0.010 1.000 1 2003 2003