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: rs1800871
rs1800871
IL10 ; IL19
108 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.010 < 0.001 1 2015 2015
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: rs8057341
rs8057341
NOD2
2 0.925 0.080 16 50704069 intron variant A/G snv 0.68 0.010 < 0.001 1 2018 2018
dbSNP: rs2430561
rs2430561
IFNG ; IFNG-AS1
50 0.590 0.760 12 68158742 intron variant T/A snv 0.36 0.020 0.500 2 2012 2014
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: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.030 1.000 3 2015 2017
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: 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: 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: rs16948876
rs16948876 		1 1.000 0.040 16 50820507 intergenic variant G/A snv 6.2E-02 0.800 1.000 2 2011 2015
dbSNP: rs2275606
rs2275606
ADGB ; LOC101928661
2 0.925 0.040 6 146597814 intron variant G/A snv 7.7E-02 0.810 1.000 2 2011 2016
dbSNP: rs3762318
rs3762318
C1orf141
3 0.925 0.040 1 67131436 intron variant G/A snv 0.83 0.810 1.000 2 2011 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: rs5743618
rs5743618
TLR1
25 0.677 0.360 4 38797027 missense variant C/A snv 0.53 0.51 0.020 1.000 2 2010 2013
dbSNP: rs606231248
rs606231248
MRC1
3 0.882 0.080 10 17849701 missense variant G/A snv 0.32 0.020 1.000 2 2010 2012
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: rs763780
rs763780
IL17F
87 0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 0.020 1.000 2 2014 2019
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: rs9356058
rs9356058
PACRG
1 1.000 0.040 6 162730367 intron variant C/A;T snv 0.020 1.000 2 2012 2013
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: rs10100465
rs10100465
LOC105375721
1 1.000 0.040 8 117614040 intergenic variant G/A snv 0.23 0.700 1.000 1 2016 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: rs10414149
rs10414149
SIGLEC5
1 1.000 0.040 19 51624491 intron variant A/G snv 0.30 0.700 1.000 1 2015 2015