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: rs1800896
rs1800896
IL10 ; IL19
113 0.507 0.800 1 206773552 intron variant T/C snv 0.41 0.030 1.000 3 2017 2019
dbSNP: rs4986790
rs4986790
TLR4
223 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.030 1.000 3 2004 2010
dbSNP: rs12979860
rs12979860
IFNL4
84 0.547 0.520 19 39248147 intron variant C/T snv 0.39 0.020 1.000 2 2012 2020
dbSNP: rs1800890
rs1800890
IL19
29 0.658 0.400 1 206776020 intron variant A/T snv 0.32 0.020 1.000 2 2017 2018
dbSNP: rs2275913
rs2275913
IL17A
105 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.020 1.000 2 2010 2018
dbSNP: rs4986791
rs4986791
TLR4
182 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 0.020 1.000 2 2004 2006
dbSNP: rs8099917
rs8099917 		60 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 0.020 1.000 2 2012 2020
dbSNP: rs1060826
rs1060826
NOS2
4 0.851 0.160 17 27762841 synonymous variant T/C snv 0.66 0.67 0.010 1.000 1 2007 2007
dbSNP: rs10735810
rs10735810
VDR
26 0.662 0.640 12 47879112 start lost A/C;G;T snv 0.010 1.000 1 2007 2007
dbSNP: rs10757212
rs10757212
IFNA5 ; LOC107987053
2 0.925 0.120 9 21304804 synonymous variant G/A snv 0.25 0.27 0.010 1.000 1 2007 2007
dbSNP: rs11650680
rs11650680 		5 0.827 0.120 17 40422984 intergenic variant C/T snv 0.17 0.010 1.000 1 2015 2015
dbSNP: rs11688
rs11688
JUN
1 1.000 0.080 1 58782321 synonymous variant C/T snv 5.3E-02 9.7E-02 0.010 1.000 1 2007 2007
dbSNP: rs12603332
rs12603332
ORMDL3 ; LRRC3C ; LOC112268187
7 0.807 0.200 17 39926554 5 prime UTR variant T/C snv 0.49 0.010 1.000 1 2015 2015
dbSNP: rs1420101
rs1420101
IL18R1 ; IL1RL1
8 0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 0.010 1.000 1 2012 2012
dbSNP: rs1799962
rs1799962
IL9
3 0.925 0.080 5 135896167 upstream gene variant T/C;G snv 7.2E-02 0.010 1.000 1 2010 2010
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2009 2009
dbSNP: rs1800871
rs1800871
IL10 ; IL19
108 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.010 1.000 1 2018 2018
dbSNP: rs1800872
rs1800872
IL10 ; IL19
119 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 0.010 1.000 1 2018 2018
dbSNP: rs1800888
rs1800888
ADRB2
23 0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 0.010 1.000 1 2015 2015
dbSNP: rs187084
rs187084
TLR9
36 0.641 0.480 3 52227015 intron variant A/G snv 0.38 0.010 1.000 1 2016 2016
dbSNP: rs1872387
rs1872387
LOC105373640
2 0.925 0.120 2 138964859 intron variant G/C snv 0.55 0.010 1.000 1 2014 2014
dbSNP: rs1921622
rs1921622
IL18R1 ; IL1RL1
2 1.000 0.080 2 102349607 intron variant G/A snv 0.42 0.010 1.000 1 2012 2012
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: rs2407992
rs2407992
TLR8 ; TLR8-AS1
4 0.882 0.200 X 12920993 synonymous variant G/A;C snv 0.54 0.010 < 0.001 1 2016 2016
dbSNP: rs3732378
rs3732378
CX3CR1
48 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2006 2006