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: rs4986790
rs4986790
TLR4
223 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.020 1.000 2 2006 2007
dbSNP: rs2069885
rs2069885
IL9
5 0.851 0.120 5 135892476 missense variant G/A;C snv 0.11 0.010 1.000 1 2010 2010
dbSNP: rs2233409
rs2233409
NFKBIA
3 1.000 0.080 14 35405064 upstream gene variant G/A snv 0.19 0.010 1.000 1 2013 2013
dbSNP: rs3760861
rs3760861
LILRB1
1 19 54630650 5 prime UTR variant A/G snv 0.64 0.010 1.000 1 2015 2015
dbSNP: rs522616
rs522616
MMP3
10 0.763 0.320 11 102844317 upstream gene variant T/C snv 0.23 0.010 1.000 1 2012 2012