rs72928038, BACH2

N. diseases: 19
Source: CURATED ×
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.
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
1789 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.810 1.000 2 2012 2016
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
363 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2016 2016
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
142 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
132 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
141 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
231 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019
Autoimmune thyroiditis
CUI: C0920350
Disease: Autoimmune thyroiditis
66 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2012 2012
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
202 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2016 2016
Cholangitis, Sclerosing
CUI: C0008313
Disease: Cholangitis, Sclerosing
276 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2016 2016
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
792 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2016 2016
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
611 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2015 2015
Graves Disease
CUI: C0018213
Disease: Graves Disease
121 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2012 2012
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
18 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2012 2012
Lymphocyte Count measurement
CUI: C0200635
Disease: Lymphocyte Count measurement
456 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2016 2016
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
637 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2013 2013
Psoriasis
CUI: C0033860
Disease: Psoriasis
501 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2016 2016
Squamous cell carcinoma
CUI: C0007137
Disease: Squamous cell carcinoma
66 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2019 2019
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
475 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2016 2016
Vitiligo
CUI: C0042900
Disease: Vitiligo
171 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2016 2016