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: rs4938573
rs4938573 		4 0.851 0.280 11 118871133 regulatory region variant C/T snv 0.79 0.700 1.000 2 2011 2012
dbSNP: rs4952108
rs4952108 		1 1.000 0.080 2 30206869 upstream gene variant C/A;T snv 0.800 1.000 2 2011 2015
dbSNP: rs545143
rs545143
IL12A-AS1
1 1.000 0.080 3 160014208 intron variant C/A;T snv 0.41 0.700 1.000 2 2012 2012
dbSNP: rs5742909
rs5742909
CTLA4
40 0.614 0.680 2 203867624 upstream gene variant C/T snv 6.7E-02 0.020 1.000 2 2010 2017
dbSNP: rs582537
rs582537
IL12A ; IL12A-AS1
1 1.000 0.080 3 159992311 intron variant A/C;G snv 0.800 1.000 2 2012 2017
dbSNP: rs622342
rs622342
SLC22A1
4 0.882 0.280 6 160151834 intron variant C/A snv 0.70 0.020 1.000 2 2014 2015
dbSNP: rs6421571
rs6421571 		6 0.851 0.200 11 118873063 intergenic variant T/A;C snv 0.800 1.000 2 2011 2015
dbSNP: rs6441286
rs6441286
IL12A-AS1
2 0.925 0.080 3 160011091 intron variant T/G snv 0.36 0.800 1.000 2 2009 2010
dbSNP: rs6478108
rs6478108
TNFSF15
10 0.763 0.200 9 114796423 intron variant C/T snv 0.73 0.710 1.000 2 2012 2016
dbSNP: rs7117261
rs7117261 		1 1.000 0.080 11 118870448 regulatory region variant T/A;C snv 0.80 0.700 1.000 2 2012 2012
dbSNP: rs715505
rs715505
SYNGR1
1 1.000 0.080 22 39355246 intron variant G/C snv 0.21 0.700 1.000 2 2012 2012
dbSNP: rs72678531
rs72678531
IL12RB2
1 1.000 0.080 1 67332762 intron variant T/C snv 0.17 0.800 1.000 2 2012 2012
dbSNP: rs7665090
rs7665090
MANBA
6 0.807 0.280 4 102630446 downstream gene variant A/G snv 0.55 0.800 1.000 2 2011 2012
dbSNP: rs8067378
rs8067378 		12 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 0.800 1.000 2 2012 2012
dbSNP: rs860413
rs860413 		2 0.925 0.080 5 35942940 upstream gene variant A/C snv 0.23 0.800 1.000 2 2011 2015
dbSNP: rs907091
rs907091
IKZF3
6 0.851 0.280 17 39765489 3 prime UTR variant C/T snv 0.47 0.700 1.000 2 2012 2012
dbSNP: rs1003643
rs1003643 		1 1.000 0.080 22 39280489 downstream gene variant T/G snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs1003644
rs1003644 		1 1.000 0.080 22 39280739 downstream gene variant G/A snv 0.31 0.700 1.000 1 2011 2011
dbSNP: rs1005999
rs1005999 		1 1.000 0.080 2 104907333 intron variant C/T snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs1008591
rs1008591 		1 1.000 0.080 19 46227357 upstream gene variant A/G snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs1008723
rs1008723
GSDMB
3 0.925 0.160 17 39910014 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1011082
rs1011082
GSDMB
1 1.000 0.080 17 39912261 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1015092
rs1015092
PLCB1
1 1.000 0.080 20 8769415 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10174098
rs10174098
ITGAV
3 0.882 0.200 2 186628015 intron variant G/A snv 0.62 0.010 1.000 1 2011 2011
dbSNP: rs10181656
rs10181656
STAT4
9 0.763 0.360 2 191105153 intron variant G/C snv 0.79 0.010 1.000 1 2014 2014