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: rs3804099
rs3804099
TLR2
40 0.627 0.680 4 153703504 synonymous variant T/C snv 0.40 0.48 0.010 1.000 1 2013 2013
dbSNP: rs3804100
rs3804100
TLR2
36 0.633 0.720 4 153704257 synonymous variant T/C snv 9.0E-02 6.7E-02 0.010 1.000 1 2013 2013
dbSNP: rs4073
rs4073
CXCL8
64 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2011 2011
dbSNP: rs4612666
rs4612666
NLRP3
10 0.763 0.440 1 247435768 intron variant T/C snv 0.65 0.010 1.000 1 2015 2015
dbSNP: rs747753882
rs747753882
TLR1
3 0.925 0.120 4 38797482 synonymous variant A/G snv 4.0E-06 2.1E-05 0.010 1.000 1 2013 2013