rs13277113, BLK

N. diseases: 18
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.
Mucocutaneous Lymph Node Syndrome
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
195 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.700 1.000 1 2012 2012
Adult type dermatomyositis
CUI: C0221056
Disease: Adult type dermatomyositis
31 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.010 1.000 1 2015 2015
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.010 1.000 1 2017 2017
Arthritis
CUI: C0003864
Disease: Arthritis
69 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.010 1.000 1 2011 2011
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.010 1.000 1 2017 2017
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.010 1.000 1 2019 2019
Diabetes Mellitus, Insulin-Dependent
954 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.010 1.000 1 2011 2011
Encephalitis, St. Louis
CUI: C0014060
Disease: Encephalitis, St. Louis
34 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.010 1.000 1 2017 2017
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.010 1.000 1 2010 2010
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.010 1.000 1 2019 2019
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.010 1.000 1 2019 2019
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.010 1.000 1 2011 2011
Primary Sjögren's syndrome
CUI: C0151449
Disease: Primary Sjögren's syndrome
42 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.010 1.000 1 2013 2013
Dermatomyositis
CUI: C0011633
Disease: Dermatomyositis
34 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.020 1.000 2 2014 2015
Polymyositis
CUI: C0085655
Disease: Polymyositis
22 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.020 1.000 2 2014 2015
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.020 1.000 2 2010 2011
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.030 1.000 3 2011 2017
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.695 0.520 8 11491677 intron variant G/A snv 0.25 0.890 1.000 13 2008 2019