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: rs1347671835
rs1347671835
IL17C
5 0.827 0.160 16 88639888 missense variant C/A;G snv 4.3E-06 0.010 1.000 1 2019 2019
dbSNP: rs149997688
rs149997688
DDR1
1 1.000 0.080 6 30893833 intron variant G/A snv 0.700 1.000 1 2019 2019
dbSNP: rs200215055
rs200215055
FCGR3B
11 0.742 0.400 1 161626196 missense variant C/A;G;T snv 1.5E-03; 1.2E-05; 4.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs281875214
rs281875214
CARD14
7 0.790 0.160 17 80183976 missense variant A/C snv 0.010 1.000 1 2019 2019
dbSNP: rs281875215
rs281875215
CARD14
6 0.807 0.160 17 80182790 missense variant G/A snv 8.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs28780111
rs28780111 		1 1.000 0.080 6 30752534 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs30187
rs30187
ERAP1
14 0.732 0.360 5 96788627 missense variant T/A;C snv 0.62 0.010 1.000 1 2016 2016
dbSNP: rs4921482
rs4921482
LOC285626
6 0.807 0.120 5 159337470 intron variant T/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs4986790
rs4986790
TLR4
223 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 0.010 1.000 1 2016 2016
dbSNP: rs71562294
rs71562294
REV3L ; TRAF3IP2-AS1
2 0.925 0.080 6 111484775 non coding transcript exon variant A/G snv 0.700 1.000 1 2019 2019
dbSNP: rs763361
rs763361
CD226
21 0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 0.010 1.000 1 2017 2017
dbSNP: rs76956521
rs76956521
TNIP1
1 1.000 0.080 5 151085080 intron variant A/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs79877597
rs79877597
IL25 ; CMTM5
2 0.925 0.080 14 23375770 missense variant C/A;T snv 0.010 1.000 1 2015 2015
dbSNP: rs145699582
rs145699582
INSL6
1 1.000 0.080 9 5169600 intron variant C/T snv 2.5E-03 0.700 1.000 1 2015 2015
dbSNP: rs34536443
rs34536443
TYK2
25 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 0.010 1.000 1 2017 2017
dbSNP: rs2066844
rs2066844
NOD2
54 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 0.020 0.500 2 2004 2006
dbSNP: rs28724231
rs28724231
HLA-DQB1 ; HLA-DQB1-AS1
1 1.000 0.080 6 32659314 upstream gene variant A/G snv 2.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs11171806
rs11171806
IL23A
7 0.807 0.360 12 56339747 synonymous variant G/A snv 4.9E-02 4.5E-02 0.010 1.000 1 2013 2013
dbSNP: rs361525
rs361525
TNF
62 0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 0.030 1.000 3 2018 2019
dbSNP: rs11209026
rs11209026
IL23R
46 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.040 1.000 4 2008 2019
dbSNP: rs13190932
rs13190932
TRAF3IP2 ; TRAF3IP2-AS1
1 1.000 0.080 6 111591867 missense variant G/A snv 5.3E-02 5.0E-02 0.710 1.000 2 2010 2019
dbSNP: rs74817271
rs74817271
TNIP1
6 0.807 0.120 5 151090412 intron variant G/A snv 5.0E-02 0.700 1.000 1 2019 2019
dbSNP: rs458017
rs458017
REV3L ; MFSD4B
2 0.925 0.080 6 111374888 missense variant T/C snv 5.9E-02 5.6E-02 0.700 1.000 1 2019 2019
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 2018 2018
dbSNP: rs13199524
rs13199524
TNXB
9 0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 0.700 1.000 1 2019 2019