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: rs121917864
rs121917864
TLR2
31 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 0.010 1.000 1 2005 2005
dbSNP: rs1040079
rs1040079
PACRG
3 0.882 0.040 6 162792995 intron variant A/G snv 0.31 0.020 1.000 2 2006 2012
dbSNP: rs2275848
rs2275848
NINJ1
2 0.925 0.120 9 93125038 missense variant G/T snv 0.81 0.77 0.010 < 0.001 1 2007 2007
dbSNP: rs3764147
rs3764147
LACC1
7 0.807 0.280 13 43883789 missense variant A/G snv 0.28 0.27 0.820 1.000 4 2009 2018
dbSNP: rs3088362
rs3088362
CCDC122
1 1.000 0.040 13 43859494 intron variant C/A;T snv 0.710 1.000 3 2009 2016
dbSNP: rs6478108
rs6478108
TNFSF15
10 0.763 0.200 9 114796423 intron variant C/T snv 0.73 0.810 1.000 3 2009 2016
dbSNP: rs10507522
rs10507522
LOC107984576
1 1.000 0.040 13 43904864 intron variant A/G snv 0.11 0.710 1.000 2 2009 2016
dbSNP: rs42490
rs42490
RIPK2
5 0.882 0.160 8 89766285 intron variant G/A snv 0.60 0.800 1.000 2 2009 2011
dbSNP: rs4833095
rs4833095
TLR1
28 0.662 0.480 4 38798089 missense variant T/C snv 0.38 0.44 0.020 1.000 2 2009 2013
dbSNP: rs7194886
rs7194886 		4 0.851 0.080 16 50691282 upstream gene variant C/T snv 0.38 0.710 1.000 2 2009 2012
dbSNP: rs9302752
rs9302752 		2 0.925 0.120 16 50685192 upstream gene variant T/C snv 0.68 0.800 1.000 2 2009 2011
dbSNP: rs9533634
rs9533634
CCDC122
1 1.000 0.040 13 43823679 downstream gene variant T/C snv 0.53 0.710 1.000 2 2009 2016
dbSNP: rs10114470
rs10114470
TNFSF15
4 0.882 0.080 9 114785492 3 prime UTR variant T/A;C snv 0.700 1.000 1 2009 2009
dbSNP: rs10982385
rs10982385 		1 1.000 0.040 9 114730737 intergenic variant T/G snv 0.47 0.700 1.000 1 2009 2009
dbSNP: rs11362
rs11362
DEFB1
13 0.742 0.360 8 6877877 5 prime UTR variant C/T snv 0.43 0.40 0.010 1.000 1 2009 2009
dbSNP: rs1800971
rs1800971
DEFB1
3 0.882 0.120 8 6870594 3 prime UTR variant T/C snv 8.0E-02 0.010 1.000 1 2009 2009
dbSNP: rs1800972
rs1800972
DEFB1
16 0.708 0.440 8 6877901 5 prime UTR variant C/G;T snv 0.79 0.010 1.000 1 2009 2009
dbSNP: rs2524132
rs2524132
HLA-B ; LINC02571 ; LOC112267902
1 1.000 0.040 6 31297135 intron variant G/A;T snv 0.700 1.000 1 2009 2009
dbSNP: rs28490179
rs28490179 		1 1.000 0.040 6 32551228 upstream gene variant C/T snv 0.81 0.700 1.000 1 2009 2009
dbSNP: rs2853930
rs2853930
HLA-B ; WASF5P
2 1.000 0.040 6 31287647 non coding transcript exon variant A/C;T snv 0.10 0.700 1.000 1 2009 2009
dbSNP: rs40457
rs40457 		1 1.000 0.040 8 89811459 intergenic variant A/G snv 0.58 0.800 1.000 1 2009 2009
dbSNP: rs4574921
rs4574921 		3 0.882 0.160 9 114776054 upstream gene variant C/T snv 0.80 0.700 1.000 1 2009 2009
dbSNP: rs602875
rs602875
HLA-DRB1
1 1.000 0.040 6 32605852 intergenic variant A/G snv 0.27 0.700 1.000 1 2009 2009
dbSNP: rs7759127
rs7759127
HLA-B ; HLA-C
5 0.925 0.040 6 31273211 intron variant T/G snv 0.11 0.700 1.000 1 2009 2009
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 2009 2009