rs11209032, None

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 0.400 1 67274409 upstream gene variant G/A snv 0.30 0.710 1.000 2 2006 2013
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 0.030 1.000 3 2012 2017
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 0.030 1.000 3 2010 2019
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 0.020 1.000 2 2015 2017
Aplastic Anemia
CUI: C0002874
Disease: Aplastic Anemia
30 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 0.010 1.000 1 2018 2018
Fuchs' syndrome
CUI: C0544015
Disease: Fuchs' syndrome
4 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 0.010 1.000 1 2010 2010
Immune thrombocytopenic purpura
CUI: C0398650
Disease: Immune thrombocytopenic purpura
35 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 0.010 1.000 1 2013 2013
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 0.010 1.000 1 2009 2009
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
47 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 0.010 1.000 1 2009 2009
Uveitis
CUI: C0042164
Disease: Uveitis
43 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 0.010 1.000 1 2017 2017