rs3024493, IL19;IL10

N. diseases: 9
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.
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 0.800 1.000 3 2009 2016
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 0.720 1.000 4 2013 2019
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 0.700 1.000 1 2016 2016
Cholangitis, Sclerosing
CUI: C0008313
Disease: Cholangitis, Sclerosing
276 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 0.700 1.000 1 2016 2016
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 0.700 1.000 1 2016 2016
Diabetes Mellitus, Insulin-Dependent
954 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 0.700 1.000 1 2011 2011
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 0.700 1.000 1 2015 2015
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 0.700 1.000 1 2016 2016
melanoma
CUI: C0025202
Disease: melanoma
515 0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 0.010 1.000 1 2015 2015