rs1129055, CD86

N. diseases: 15
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.
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.020 0.500 2 2018 2019
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.020 0.500 2 2018 2019
Acute GVH disease
CUI: C0856825
Disease: Acute GVH disease
49 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.010 1.000 1 2018 2018
Brucellosis
CUI: C0006309
Disease: Brucellosis
30 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.010 1.000 1 2014 2014
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.010 1.000 1 2010 2010
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.010 1.000 1 2014 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.010 1.000 1 2010 2010
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.010 1.000 1 2014 2014
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.010 1.000 1 2012 2012
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.010 1.000 1 2014 2014
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
322 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.010 1.000 1 2012 2012
Pemphigus Foliaceus
CUI: C0263313
Disease: Pemphigus Foliaceus
16 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.010 1.000 1 2017 2017
Pemphigus Vulgaris
CUI: C0030809
Disease: Pemphigus Vulgaris
39 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.010 1.000 1 2017 2017
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.010 1.000 1 2014 2014
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.724 0.400 3 122119472 missense variant G/A snv 0.30 0.25 0.010 1.000 1 2013 2013