rs6478109, TNFSF15

N. diseases: 12
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 9 114806486 upstream gene variant A/G snv 0.74 0.830 1.000 7 2005 2016
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 0.800 1.000 1 2008 2008
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 0.020 1.000 2 2014 2014
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 0.010 1 2015 2015
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 0.010 1.000 1 2019 2019
Diverticulitis
CUI: C0012813
Disease: Diverticulitis
13 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 0.010 1.000 1 2017 2017
Leprosy
CUI: C0023343
Disease: Leprosy
120 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 0.010 1.000 1 2016 2016
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 0.010 1.000 1 2019 2019
Lupus Nephritis
CUI: C0024143
Disease: Lupus Nephritis
64 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 0.010 1.000 1 2019 2019
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 0.010 1.000 1 2016 2016
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 0.010 1.000 1 2014 2014
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.752 0.320 9 114806486 upstream gene variant A/G snv 0.74 0.010 1 2019 2019