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: rs3024505
rs3024505 		10 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 0.840 0.889 9 2008 2017
dbSNP: rs6426833
rs6426833 		6 0.827 0.120 1 19845367 TF binding site variant G/A snv 0.52 0.810 1.000 9 2009 2017
dbSNP: rs17085007
rs17085007 		7 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 0.820 1.000 8 2009 2017
dbSNP: rs4728142
rs4728142 		18 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 0.820 1.000 7 2011 2017
dbSNP: rs10758669
rs10758669 		10 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.830 1.000 6 2010 2016
dbSNP: rs2542151
rs2542151 		11 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 0.060 1.000 6 2012 2016
dbSNP: rs1004819
rs1004819
IL23R ; C1orf141
9 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.050 0.800 5 2007 2017
dbSNP: rs2275913
rs2275913
IL17A
105 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 0.050 1.000 5 2008 2014
dbSNP: rs6017342
rs6017342
LINC01620
3 0.925 0.120 20 44436388 non coding transcript exon variant A/C snv 0.62 0.810 1.000 5 2009 2017
dbSNP: rs6478108
rs6478108
TNFSF15
10 0.763 0.200 9 114796423 intron variant C/T snv 0.73 0.050 1.000 5 2014 2018
dbSNP: rs2395185
rs2395185
HLA-DRB9
17 0.724 0.360 6 32465390 intron variant G/T snv 0.29 0.810 1.000 4 2009 2012
dbSNP: rs254560
rs254560
C5orf66
2 1.000 0.040 5 135107916 intron variant G/A snv 0.32 0.800 1.000 4 2011 2017
dbSNP: rs2816958
rs2816958
NR5A2
6 0.827 0.120 1 200132792 intron variant A/G snv 0.84 0.800 1.000 4 2012 2017
dbSNP: rs2836878
rs2836878 		7 0.851 0.200 21 39093608 intergenic variant G/A snv 0.23 0.800 1.000 4 2010 2017
dbSNP: rs3806308
rs3806308
RNF186
5 0.827 0.120 1 19816373 intron variant C/T snv 0.36 0.800 1.000 4 2009 2016
dbSNP: rs7517847
rs7517847
IL23R ; C1orf141
19 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.730 1.000 4 2008 2016
dbSNP: rs7554511
rs7554511
INAVA
3 0.925 0.040 1 200908434 intron variant C/A snv 0.22 0.800 1.000 4 2009 2017
dbSNP: rs7574865
rs7574865
STAT4
59 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.040 0.750 4 2008 2015
dbSNP: rs7608910
rs7608910
PUS10
6 0.827 0.120 2 60977721 intron variant A/G snv 0.37 0.800 1.000 4 2011 2017
dbSNP: rs7848647
rs7848647
TNFSF15
13 0.732 0.320 9 114806766 upstream gene variant T/C snv 0.74 0.730 1.000 4 2014 2018
dbSNP: rs941823
rs941823
LINC00598
6 0.827 0.120 13 40439840 intron variant T/C snv 0.77 0.800 1.000 4 2011 2017
dbSNP: rs10754558
rs10754558
NLRP3
20 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 0.030 1.000 3 2014 2018
dbSNP: rs10883365
rs10883365
LINC01475
3 0.882 0.080 10 99528007 non coding transcript exon variant G/A snv 0.52 0.030 1.000 3 2010 2014
dbSNP: rs10889677
rs10889677
IL23R
40 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 0.820 1.000 3 2009 2020
dbSNP: rs11150589
rs11150589
ITGAL
2 1.000 0.040 16 30471173 upstream gene variant T/A;C;G snv 0.800 1.000 3 2012 2017