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: 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: 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: 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: 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
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: rs2201841
rs2201841
IL23R ; C1orf141
0.716 0.440 1 67228519 intron variant A/G;T snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.820 1.000 1 2010 2017
dbSNP: rs2201841
rs2201841
IL23R ; C1orf141
0.716 0.440 1 67228519 intron variant A/G;T snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.830 1.000 1 2009 2016
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: rs2295359
rs2295359
IL23R ; C1orf141
1.000 0.040 1 67170267 intron variant G/A snv 0.32
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2015 2015
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: rs4655683
rs4655683
IL23R ; C1orf141
1.000 0.080 1 67145930 intron variant G/A snv 0.37
CUI: C0003872
Disease: Arthritis, Psoriatic
Arthritis, Psoriatic 		0.700 1.000 1 2019 2019
dbSNP: rs7517847
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.730 1.000 1 2008 2016
dbSNP: rs7517847
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37
CUI: C0008313
Disease: Cholangitis, Sclerosing
Cholangitis, Sclerosing 		0.700 1.000 1 2016 2016
dbSNP: rs7517847
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.700 1.000 1 2016 2016
dbSNP: rs7517847
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.720 1.000 1 2012 2018
dbSNP: rs76418789
rs76418789
IL23R ; C1orf141
0.882 0.080 1 67182913 missense variant G/A snv 7.3E-03 4.5E-03
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.710 1.000 1 2016 2016