rs11465804, IL23R

N. diseases: 10
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 0.800 1.000 5 2006 2010
Asthma
CUI: C0004096
Disease: Asthma
1536 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 0.700 1.000 1 2011 2011
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 0.700 1.000 1 2011 2011
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 0.020 1.000 2 2012 2018
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
52 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 0.010 1.000 1 2019 2019
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 0.010 1.000 1 2009 2009
Sarcoidosis
CUI: C0036202
Disease: Sarcoidosis
787 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 0.010 1.000 1 2011 2011
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 0.010 1.000 1 2009 2009
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 0.010 1.000 1 2017 2017
Uveitis
CUI: C0042164
Disease: Uveitis
43 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 0.010 1.000 1 2011 2011