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: rs10513854
rs10513854
IL1RAP
1 3 190588085 intron variant C/T snv 0.18 0.010 1.000 1 2014 2014
dbSNP: rs17639215
rs17639215
IL18R1 ; IL1RL1
1 2 102336984 intron variant G/A snv 9.7E-02 0.010 1.000 1 2014 2014
dbSNP: rs2230804
rs2230804
CHUK
1 10 100218126 missense variant C/T snv 0.47 0.57 0.010 1.000 1 2014 2014
dbSNP: rs3024492
rs3024492
IL10 ; IL19
1 1 206770767 5 prime UTR variant T/A snv 0.17 0.010 1.000 1 2013 2013
dbSNP: rs3093664
rs3093664
TNF
2 6 31576865 intron variant A/G snv 6.9E-02 7.7E-02 0.010 1.000 1 2016 2016
dbSNP: rs7037276
rs7037276
IL33 ; LOC107987046
1 9 6247430 intron variant C/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs9290936
rs9290936
IL1RAP
1 3 190534846 intron variant G/T snv 0.20 0.010 1.000 1 2014 2014
dbSNP: rs9892651
rs9892651
PRKCA
2 17 66307675 intron variant C/T snv 0.59 0.010 1.000 1 2016 2016
dbSNP: rs4807000
rs4807000
TICAM1
2 1.000 0.040 19 4831866 upstream gene variant A/G snv 0.67 0.010 1.000 1 2014 2014
dbSNP: rs4742170
rs4742170
IL33 ; LOC107987046
3 0.925 0.080 9 6242950 intron variant C/G;T snv 0.020 0.500 2 2014 2018
dbSNP: rs146855738
rs146855738
HNF1A ; C12orf43
2 1.000 0.080 12 121001145 missense variant G/A;C snv 3.6E-05; 4.0E-06; 8.0E-06 5.6E-05 0.010 1.000 1 2008 2008
dbSNP: rs2569191
rs2569191
CD14 ; TMCO6
2 1.000 0.080 5 140634318 upstream gene variant C/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs2806489
rs2806489
CYSLTR1
2 1.000 0.080 X 78327951 upstream gene variant C/T snv 0.010 < 0.001 1 2009 2009
dbSNP: rs3742030
rs3742030
TRPV4
4 0.925 0.080 12 109814742 missense variant G/A;C snv 3.7E-02 0.010 < 0.001 1 2010 2010
dbSNP: rs408223
rs408223
CDHR3
2 1.000 0.080 7 106021578 intron variant C/G snv 0.27 0.010 1.000 1 2020 2020
dbSNP: rs5030411
rs5030411
RAG1 ; TRAF6
2 1.000 0.080 11 36512203 intron variant G/A snv 0.49 0.010 1.000 1 2014 2014
dbSNP: rs6967330
rs6967330
CDHR3
8 0.827 0.120 7 106018005 missense variant G/A snv 0.19 0.21 0.040 1.000 4 2015 2020
dbSNP: rs2280090
rs2280090
ADAM33
4 0.882 0.120 20 3669558 missense variant G/A snv 0.13 0.14 0.010 1.000 1 2016 2016
dbSNP: rs3918396
rs3918396
ADAM33
5 0.851 0.120 20 3671118 missense variant C/T snv 5.1E-05; 7.6E-02 6.7E-02 0.010 1.000 1 2016 2016
dbSNP: rs4129009
rs4129009
TLR10
6 0.882 0.120 4 38773268 missense variant T/A;C;G snv 0.17 0.13 0.010 1.000 1 2016 2016
dbSNP: rs528557
rs528557
ADAM33
6 0.827 0.120 20 3671095 synonymous variant C/A;G snv 4.7E-06; 0.29 0.010 < 0.001 1 2015 2015
dbSNP: rs2915863
rs2915863
CD14 ; TMCO6
3 0.925 0.160 5 140634792 upstream gene variant C/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs2981573
rs2981573
IL20
4 0.882 0.160 1 206867232 intron variant G/A snv 0.77 0.010 1.000 1 2011 2011
dbSNP: rs8113232
rs8113232
GIPC3
3 0.925 0.160 19 3586545 synonymous variant G/A snv 4.0E-06; 0.14 0.24 0.010 1.000 1 2012 2012
dbSNP: rs10938397
rs10938397 		19 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 0.010 1.000 1 2016 2016