Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs11465804
rs11465804
IL23R
0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 4 2006 2010
dbSNP: rs17234657
rs17234657 		0.882 0.120 5 40401407 intergenic variant T/G snv 0.14
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 2 2007 2010
dbSNP: rs17309827
rs17309827
SLC22A23
1.000 0.040 6 3433084 intron variant T/G snv 0.30
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 2 2008 2010
dbSNP: rs1063355
rs1063355
HLA-DQB1 ; HLA-DQB1-AS1
0.827 0.320 6 32659937 3 prime UTR variant T/G snv 0.56
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2013 2013
dbSNP: rs17582416
rs17582416 		0.882 0.160 10 34998722 regulatory region variant T/G snv 0.31
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2008 2008
dbSNP: rs17695092
rs17695092
CPEB4
1.000 0.040 5 173910850 intron variant T/G snv 0.22
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2012 2012
dbSNP: rs3135503
rs3135503
CYLD
1.000 0.040 16 50757339 intron variant T/G snv 0.32
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2007 2007
dbSNP: rs4372078
rs4372078
TNFSF15
1.000 0.040 9 114801407 intron variant T/G snv 0.78
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2005 2005
dbSNP: rs72981516
rs72981516
FCHSD2
1.000 0.040 11 72959855 intron variant T/G snv 6.2E-05
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2013 2013
dbSNP: rs751271
rs751271
NOD2
1.000 0.040 16 50717264 intron variant T/G snv 0.61
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2007 2007
dbSNP: rs7517847
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.880 1.000 1 2007 2019
dbSNP: rs751919
rs751919
CYLD ; MIR3181 ; LOC102724907
1.000 0.040 16 50741834 intron variant T/G snv 0.35
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2007 2007
dbSNP: rs7765379
rs7765379 		0.827 0.280 6 32713151 upstream gene variant T/G snv 0.10
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 1 2013 2013
dbSNP: rs11742570
rs11742570 		0.925 0.040 5 40410482 upstream gene variant T/C;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 2 2010 2017
dbSNP: rs6716753
rs6716753
SP140
1.000 0.040 2 230232414 intron variant T/C;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2012 2017
dbSNP: rs13361189
rs13361189 		0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 1.000 2 2007 2015
dbSNP: rs3810936
rs3810936
TNFSF15
0.742 0.320 9 114790605 synonymous variant T/C snv 0.71 0.75
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 1.000 2 2005 2018
dbSNP: rs4613763
rs4613763 		0.851 0.240 5 40392626 regulatory region variant T/C snv 0.14
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 2 2007 2008
dbSNP: rs6651252
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 2 2010 2019
dbSNP: rs6908425
rs6908425
CDKAL1
0.752 0.320 6 20728500 intron variant T/C snv 0.78
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 2 2008 2015
dbSNP: rs1002922
rs1002922 		1.000 0.040 5 40386453 regulatory region variant T/C snv 0.29
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2007 2007
dbSNP: rs102275
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 1 2010 2018
dbSNP: rs10489629
rs10489629
IL23R ; C1orf141
0.827 0.240 1 67222666 intron variant T/C snv 0.48
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2006 2006
dbSNP: rs11190140
rs11190140
NKX2-3 ; LINC01475
0.827 0.160 10 99531836 upstream gene variant T/C snv 0.55
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 1 2008 2014
dbSNP: rs11209002
rs11209002
C1orf141
1.000 0.040 1 67124778 intron variant T/C snv 0.77
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2007 2007