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: rs3122929
rs3122929
STAT6
4 0.882 0.080 12 57115319 intron variant C/T snv 0.33 0.700 1.000 3 2019 2019
dbSNP: rs72743461
rs72743461
SMAD3
6 0.827 0.160 15 67149412 intron variant C/A;T snv 0.700 1.000 3 2019 2019
dbSNP: rs72823641
rs72823641
IL18R1 ; IL1RL1
4 0.882 0.080 2 102319699 intron variant T/A;C snv 0.700 1.000 3 2018 2019
dbSNP: rs7936312
rs7936312 		5 0.882 0.080 11 76582682 intergenic variant G/T snv 0.44 0.700 1.000 3 2019 2019
dbSNP: rs10187276
rs10187276 		2 0.925 0.080 2 227805721 upstream gene variant T/C snv 0.62 0.700 1.000 2 2019 2019
dbSNP: rs10208293
rs10208293
IL18R1 ; IL1RL1
4 0.882 0.160 2 102349850 intron variant G/A snv 0.33 0.700 1.000 2 2016 2019
dbSNP: rs10519068
rs10519068
RORA
2 0.925 0.120 15 60776505 intron variant G/A snv 0.22 0.700 1.000 2 2016 2019
dbSNP: rs1059513
rs1059513
NAB2 ; STAT6
11 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 0.700 1.000 2 2018 2019
dbSNP: rs10903122
rs10903122 		5 0.882 0.200 1 24977085 intergenic variant A/G snv 0.56 0.700 1.000 2 2011 2011
dbSNP: rs112401631
rs112401631 		8 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 0.700 1.000 2 2019 2019
dbSNP: rs117710327
rs117710327 		5 0.882 0.080 19 33235672 TF binding site variant C/A snv 5.0E-02 0.700 1.000 2 2019 2019
dbSNP: rs11778371
rs11778371
CHRNA2
1 1.000 0.080 8 27462388 intron variant C/T snv 4.0E-02 0.700 1.000 2 2009 2010
dbSNP: rs12123821
rs12123821
FLG-AS1 ; LOC112268240
4 0.925 0.080 1 152206676 intron variant C/T snv 2.9E-02 0.700 1.000 2 2019 2019
dbSNP: rs12150079
rs12150079
ZPBP2
9 0.807 0.280 17 39869164 intron variant G/A snv 0.24 0.700 1.000 2 2010 2011
dbSNP: rs12722502
rs12722502
IL2RA
4 0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 0.700 1.000 2 2019 2019
dbSNP: rs13277355
rs13277355 		3 0.882 0.120 8 127765473 intergenic variant A/G snv 0.71 0.700 1.000 2 2019 2019
dbSNP: rs13314993
rs13314993
LOC105377022
5 0.882 0.200 3 32973977 regulatory region variant G/C;T snv 0.700 1.000 2 2011 2011
dbSNP: rs13431828
rs13431828
IL18R1 ; IL1RL1
3 0.925 0.160 2 102338193 5 prime UTR variant C/T snv 0.18 0.700 1.000 2 2010 2011
dbSNP: rs144829310
rs144829310 		2 1.000 0.080 9 6208030 intergenic variant G/T snv 0.12 0.700 1.000 2 2016 2019
dbSNP: rs1464510
rs1464510
LPP
9 0.807 0.280 3 188394766 intron variant C/A;T snv 0.700 1.000 2 2011 2011
dbSNP: rs1684466
rs1684466
LINC01063
2 1.000 0.080 3 196632439 non coding transcript exon variant G/A;C snv 0.700 1.000 2 2019 2019
dbSNP: rs16903574
rs16903574
OTULINL
6 0.882 0.120 5 14610200 missense variant C/A;G snv 4.0E-06; 5.6E-02 0.700 1.000 2 2019 2019
dbSNP: rs1736135
rs1736135
LOC101927745
4 0.851 0.160 21 15432901 intron variant T/C snv 0.33 0.700 1.000 2 2011 2011
dbSNP: rs1810132
rs1810132
ERBB2
1 1.000 0.080 17 39709752 intron variant C/T snv 0.64 0.700 1.000 2 2010 2011
dbSNP: rs2070901
rs2070901
FCER1G
4 0.882 0.120 1 161215268 non coding transcript exon variant G/T snv 0.32 0.700 1.000 2 2019 2019