Source: GWASDB ×
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: rs1295686
rs1295686
IL13 ; TH2LCRR
2 0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 0.840 1.000 3 2010 2018
dbSNP: rs1588265
rs1588265
PDE4D
1 1.000 0.080 5 60073967 intron variant A/G;T snv 0.800 1.000 3 2009 2011
dbSNP: rs2872507
rs2872507 		7 0.752 0.360 17 39884510 intergenic variant G/A;T snv 0.720 1.000 3 2010 2012
dbSNP: rs3771166
rs3771166
IL18R1
2 1.000 0.080 2 102369762 intron variant G/A;T snv 0.810 1.000 3 2010 2012
dbSNP: rs744910
rs744910
SMAD3
1 1.000 0.080 15 67154447 intron variant G/A;T snv 0.810 1.000 3 2010 2012
dbSNP: rs9273349
rs9273349
HLA-DQB1-AS1
1 0.827 0.200 6 32658092 upstream gene variant T/C;G snv 0.810 1.000 3 2010 2012
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: rs1464510
rs1464510
LPP
7 0.807 0.280 3 188394766 intron variant C/A;T snv 0.700 1.000 2 2011 2011
dbSNP: rs4794820
rs4794820
LRRC3C
3 0.790 0.160 17 39933091 intron variant A/G;T snv 0.810 1.000 2 2011 2012
dbSNP: rs4795405
rs4795405
LRRC3C
3 0.851 0.160 17 39932164 intron variant T/A;C snv 0.720 1.000 2 2010 2013
dbSNP: rs6503525
rs6503525
LRRC3C
2 0.925 0.080 17 39938921 intron variant G/A;C snv 0.810 1.000 2 2011 2015
dbSNP: rs802734
rs802734 		5 0.827 0.280 6 127957653 intergenic variant A/G;T snv 0.700 1.000 2 2011 2011
dbSNP: rs1008723
rs1008723
GSDMB
3 0.925 0.160 17 39910014 intron variant G/C;T snv 0.800 1.000 1 2011 2019
dbSNP: rs10204137
rs10204137
IL18R1 ; IL1RL1
1 0.925 0.160 2 102351752 missense variant A/G;T snv 0.34 0.700 1.000 1 2010 2010
dbSNP: rs10206753
rs10206753
IL18R1 ; IL1RL1
2 1.000 0.080 2 102351902 missense variant T/C;G snv 0.34; 4.0E-06 0.700 1.000 1 2010 2010
dbSNP: rs1043828
rs1043828
WDR36
2 1.000 0.080 5 111128310 3 prime UTR variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs10758669
rs10758669 		5 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs11221332
rs11221332
ETS1
5 0.763 0.280 11 128511079 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs11242168
rs11242168
FSTL4
1 1.000 0.080 5 133667444 intergenic variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs11252191
rs11252191
LINC02660
1 1.000 0.080 10 3921969 intron variant C/A;G;T snv 0.700 1.000 1 2014 2014
dbSNP: rs113612868
rs113612868
TCAP
1 1.000 0.080 17 39665182 upstream gene variant -/T ins 0.700 1.000 1 2010 2010
dbSNP: rs1229598
rs1229598 		1 1.000 0.080 18 56267556 regulatory region variant A/C;G;T snv 0.700 1.000 1 2000 2000
dbSNP: rs1250552
rs1250552
ZMIZ1
5 0.882 0.200 10 79298270 intron variant A/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs12936231
rs12936231
ZPBP2
3 0.925 0.160 17 39872867 intron variant C/G;T snv 0.720 1.000 1 2011 2019
dbSNP: rs13010713
rs13010713
LINC01934
5 0.882 0.200 2 181131318 intron variant A/C;G snv 0.700 1.000 1 2011 2011