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: rs1801274
rs1801274
FCGR2A
46 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.020 1.000 2 2014 2015
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 2015 2015
dbSNP: rs8192284
rs8192284
IL6R
19 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2019 2019
dbSNP: rs1143627
rs1143627
IL1B
47 0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 0.010 1.000 1 2014 2014
dbSNP: rs371057322
rs371057322
KIDINS220
2 0.925 0.040 2 8793960 missense variant T/C snv 1.4E-05 0.010 1.000 1 2007 2007
dbSNP: rs6141
rs6141
THPO
4 0.925 0.080 3 184372478 3 prime UTR variant C/G;T snv 4.0E-06; 0.56 0.010 1.000 1 2016 2016
dbSNP: rs3775291
rs3775291
TLR3
51 0.602 0.640 4 186082920 missense variant C/G;T snv 1.2E-04; 0.28 0.010 1.000 1 2015 2015
dbSNP: rs4859584
rs4859584
ART3 ; CXCL10
1 1.000 0.040 4 76021984 intron variant G/C snv 0.61 0.61 0.010 1.000 1 2015 2015
dbSNP: rs750898115
rs750898115
USO1
4 0.882 0.080 4 75787191 missense variant A/G snv 1.0E-05 3.5E-05 0.010 1.000 1 2007 2007
dbSNP: rs1799964
rs1799964
LTA ; TNF ; LOC100287329
47 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 0.020 1.000 2 2013 2015
dbSNP: rs3132468
rs3132468
MICB
5 0.827 0.240 6 31507709 intron variant C/T snv 0.77 0.020 0.500 2 2013 2014
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 2013 2013
dbSNP: rs5745568
rs5745568
BAK1 ; GGNBP1
4 0.882 0.080 6 33580617 intron variant G/T snv 0.19 0.010 1.000 1 2016 2016
dbSNP: rs763780
rs763780
IL17F
87 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 0.010 1.000 1 2015 2015
dbSNP: rs1285933
rs1285933
MGAM ; CLEC5A
2 0.925 0.040 7 141927349 intron variant G/A snv 0.54 0.010 1.000 1 2017 2017
dbSNP: rs1799983
rs1799983
NOS3
246 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 0.010 1.000 1 2019 2019
dbSNP: rs3739319
rs3739319
IDO1
2 0.925 0.040 8 39927802 intron variant G/A snv 0.40 0.37 0.010 1.000 1 2019 2019
dbSNP: rs3205166
rs3205166
DDX58
2 0.925 0.040 9 32459452 synonymous variant T/A;G snv 0.35 0.010 1.000 1 2015 2015
dbSNP: rs385893
rs385893 		9 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 0.010 1.000 1 2016 2016
dbSNP: rs669260
rs669260
DDX58
4 0.851 0.080 9 32503442 intron variant T/A;C snv 0.010 1.000 1 2015 2015
dbSNP: rs1447043692
rs1447043692
HPSE2
2 0.925 0.040 10 98641918 missense variant C/T snv 0.010 1.000 1 2007 2007
dbSNP: rs3740360
rs3740360
PLCE1
7 0.827 0.240 10 94265734 intron variant A/C snv 9.7E-02 8.4E-02 0.010 < 0.001 1 2013 2013
dbSNP: rs3765524
rs3765524
PLCE1
17 0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 0.010 1.000 1 2014 2014
dbSNP: rs12252
rs12252
IFITM3
23 0.695 0.240 11 320772 splice region variant A/G snv 0.13 0.13 0.010 1.000 1 2019 2019
dbSNP: rs8177374
rs8177374
TIRAP
22 0.672 0.520 11 126292948 missense variant C/T snv 0.12 0.11 0.010 1.000 1 2015 2015