Source: GWASCAT

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: rs11465802
rs11465802
IL23R ; C1orf141
1.000 0.040 1 67219915 intron variant A/C;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2007 2007
dbSNP: rs1343151
rs1343151
IL23R
0.752 0.400 1 67253446 intron variant G/A snv 0.41
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2006 2007
dbSNP: rs2064689
rs2064689
IL23R ; C1orf141
1.000 0.040 1 67187327 intron variant G/A snv 0.29
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2007 2007
dbSNP: rs2902440
rs2902440
IL23R ; C1orf141
1.000 0.040 1 67205233 intron variant G/A snv 0.37
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2007 2007
dbSNP: rs9988642
rs9988642
IL23R
0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.800 1.000 1 2007 2007
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 3 2006 2010
dbSNP: rs11805303
rs11805303
IL23R ; C1orf141
0.827 0.240 1 67209833 intron variant C/T snv 0.30
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.810 1.000 1 2007 2012
dbSNP: rs9988642
rs9988642
IL23R
0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.800 1.000 1 2012 2012
dbSNP: rs2201841
rs2201841
IL23R ; C1orf141
0.716 0.440 1 67228519 intron variant A/G;T snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.850 1.000 1 2006 2013
dbSNP: rs117633859
rs117633859
IL23R ; C1orf141
1.000 0.120 1 67162145 intron variant A/G snv 2.6E-02
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
Uveomeningoencephalitic Syndrome 		0.710 1.000 1 2014 2014
dbSNP: rs11580078
rs11580078
IL23R ; C1orf141
0.724 0.240 1 67203951 intron variant C/A;G snv
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2015 2015
dbSNP: rs11580078
rs11580078
IL23R ; C1orf141
0.724 0.240 1 67203951 intron variant C/A;G snv
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases 		0.700 1.000 1 2015 2015
dbSNP: rs11580078
rs11580078
IL23R ; C1orf141
0.724 0.240 1 67203951 intron variant C/A;G snv
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6 		0.700 1.000 1 2015 2015
dbSNP: rs11580078
rs11580078
IL23R ; C1orf141
0.724 0.240 1 67203951 intron variant C/A;G snv
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2 		0.700 1.000 1 2015 2015
dbSNP: rs11580078
rs11580078
IL23R ; C1orf141
0.724 0.240 1 67203951 intron variant C/A;G snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.700 1.000 1 2015 2015
dbSNP: rs11580078
rs11580078
IL23R ; C1orf141
0.724 0.240 1 67203951 intron variant C/A;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.700 1.000 1 2015 2015
dbSNP: rs11580078
rs11580078
IL23R ; C1orf141
0.724 0.240 1 67203951 intron variant C/A;G snv
CUI: C0009447
Disease: Common Variable Immunodeficiency
Common Variable Immunodeficiency 		0.700 1.000 1 2015 2015
dbSNP: rs11580078
rs11580078
IL23R ; C1orf141
0.724 0.240 1 67203951 intron variant C/A;G snv
CUI: C0920350
Disease: Autoimmune thyroiditis
Autoimmune thyroiditis 		0.700 1.000 1 2015 2015
dbSNP: rs11580078
rs11580078
IL23R ; C1orf141
0.724 0.240 1 67203951 intron variant C/A;G snv
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2015 2015
dbSNP: rs11580078
rs11580078
IL23R ; C1orf141
0.724 0.240 1 67203951 intron variant C/A;G snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.700 1.000 1 2015 2015
dbSNP: rs11580078
rs11580078
IL23R ; C1orf141
0.724 0.240 1 67203951 intron variant C/A;G snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015
dbSNP: rs11580078
rs11580078
IL23R ; C1orf141
0.724 0.240 1 67203951 intron variant C/A;G snv
CUI: C3495559
Disease: Juvenile arthritis
Juvenile arthritis 		0.700 1.000 1 2015 2015
dbSNP: rs11580078
rs11580078
IL23R ; C1orf141
0.724 0.240 1 67203951 intron variant C/A;G snv
CUI: C0007570
Disease: Celiac Disease
Celiac Disease 		0.700 1.000 1 2015 2015
dbSNP: rs11580078
rs11580078
IL23R ; C1orf141
0.724 0.240 1 67203951 intron variant C/A;G snv
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1 		0.700 1.000 1 2015 2015
dbSNP: rs12564022
rs12564022
IL23R ; C1orf141
1.000 0.040 1 67205072 intron variant C/T snv 0.30
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015