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: rs7999279
rs7999279 		1 1.000 0.200 13 47376590 intergenic variant A/C snv 0.76 0.700 1.000 1 2017 2017
dbSNP: rs9271573
rs9271573 		1 1.000 0.200 6 32622724 TF binding site variant A/C snv 0.55 0.700 1.000 1 2017 2017
dbSNP: rs485497
rs485497
IL12A-AS1
2 0.925 0.200 3 160001345 intron variant A/C;G snv 0.700 1.000 1 2013 2013
dbSNP: rs8192284
rs8192284
IL6R
19 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2011 2011
dbSNP: rs115575857
rs115575857 		1 1.000 0.200 6 32691868 regulatory region variant A/G snv 0.700 1.000 1 2013 2013
dbSNP: rs2736345
rs2736345
BLK
3 0.882 0.280 8 11494976 intron variant A/G snv 0.35 0.700 1.000 1 2013 2013
dbSNP: rs3135394
rs3135394
HLA-DRA
4 0.851 0.240 6 32440720 intron variant A/G snv 6.3E-02 0.700 1.000 1 2013 2013
dbSNP: rs2201841
rs2201841
IL23R ; C1orf141
14 0.716 0.440 1 67228519 intron variant A/G;T snv 0.010 1.000 1 2009 2009
dbSNP: rs2431098
rs2431098 		5 0.827 0.240 5 160460329 intron variant A/G;T snv 0.700 1.000 1 2013 2013
dbSNP: rs10553577
rs10553577
STAT4
1 1.000 0.200 2 191090464 intron variant ATAATA/-;ATA;ATAATAATA delins 0.700 1.000 1 2013 2013
dbSNP: rs10889677
rs10889677
IL23R
40 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 0.010 1.000 1 2009 2009
dbSNP: rs1507153
rs1507153 		1 1.000 0.200 6 78774669 intergenic variant C/A snv 0.32 0.700 1.000 1 2013 2013
dbSNP: rs17074492
rs17074492
LOC105370283
1 1.000 0.200 13 81587764 intergenic variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs5029939
rs5029939
TNFAIP3
19 0.701 0.440 6 137874586 intron variant C/G snv 0.13 0.800 1.000 1 2013 2013
dbSNP: rs117026326
rs117026326
GTF2I ; LOC101926943
10 0.752 0.440 7 74711703 intron variant C/T snv 1.3E-02 0.800 1.000 2 2013 2016
dbSNP: rs10168266
rs10168266
STAT4
8 0.776 0.400 2 191071078 intron variant C/T snv 0.19 0.800 1.000 1 2013 2013
dbSNP: rs116855232
rs116855232
NUDT15
12 0.742 0.400 13 48045719 missense variant C/T snv 2.8E-02 1.1E-02 0.010 1.000 1 2018 2018
dbSNP: rs11805303
rs11805303
IL23R ; C1orf141
6 0.827 0.240 1 67209833 intron variant C/T snv 0.30 0.010 1.000 1 2009 2009
dbSNP: rs11889341
rs11889341
STAT4
12 0.732 0.480 2 191079016 intron variant C/T snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs17339836
rs17339836
TNPO3
1 1.000 0.200 7 129041008 intron variant C/T snv 9.0E-02 0.700 1.000 1 2013 2013
dbSNP: rs1957173
rs1957173 		1 1.000 0.200 14 45937713 intron variant C/T snv 4.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs359457
rs359457 		2 0.925 0.240 5 173852839 intergenic variant C/T snv 0.59 0.700 1.000 1 2013 2013
dbSNP: rs774359492
rs774359492
WDHD1
7 0.807 0.200 14 55008684 missense variant C/T snv 4.0E-06 7.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs9277554
rs9277554
HLA-DPB1
7 0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 0.700 1.000 1 2017 2017
dbSNP: rs1004819
rs1004819
IL23R ; C1orf141
9 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.010 1.000 1 2009 2009