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: 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: rs4282438
rs4282438
COL11A2P1
6 0.807 0.280 6 33104395 intron variant T/G snv 3.1E-02 0.800 1.000 1 2013 2013
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: rs9271588
rs9271588 		6 0.925 0.200 6 32623176 TF binding site variant T/C snv 0.43 0.800 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: rs11048434
rs11048434
KLRG1
1 1.000 0.200 12 9001336 intron variant G/A snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs115575857
rs115575857 		1 1.000 0.200 6 32691868 regulatory region variant A/G snv 0.700 1.000 1 2013 2013
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: 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: 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: rs2431098
rs2431098 		5 0.827 0.240 5 160460329 intron variant A/G;T 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: rs359457
rs359457 		2 0.925 0.240 5 173852839 intergenic variant C/T snv 0.59 0.700 1.000 1 2013 2013
dbSNP: rs3757387
rs3757387
IRF5
6 0.851 0.280 7 128936032 upstream gene variant T/C snv 0.38 0.700 1.000 1 2013 2013
dbSNP: rs3823536
rs3823536
IRF5
2 0.925 0.280 7 128939612 intron variant G/A snv 0.40 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: rs6579837
rs6579837
TNIP1
1 1.000 0.200 5 151055333 intron variant G/T snv 0.11 0.700 1.000 1 2013 2013
dbSNP: rs6933404
rs6933404 		5 0.925 0.280 6 137638098 intergenic variant T/C snv 0.16 0.700 1.000 1 2013 2013
dbSNP: rs7119038
rs7119038 		1 1.000 0.200 11 118867572 intergenic variant G/A snv 0.77 0.700 1.000 1 2013 2013
dbSNP: rs7341475
rs7341475
RELN
6 0.851 0.240 7 103764368 intron variant G/A snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs7574865
rs7574865
STAT4
59 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.700 1.000 1 2017 2017