rs1805010, IL4R

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.
ACQUIRED IMMUNODEFICIENCY SYNDROME, SLOW PROGRESSION TO
CUI: C1840084
Disease: ACQUIRED IMMUNODEFICIENCY SYNDROME, SLOW PROGRESSION TO
1 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 0.700 0
Early Rheumatoid Arthritis
CUI: C3899278
Disease: Early Rheumatoid Arthritis
5 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 0.010 1.000 1 2010 2010
Malignant neoplasm of kidney
CUI: C0740457
Disease: Malignant neoplasm of kidney
22 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 0.010 1.000 1 2012 2012
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 0.010 1.000 1 2012 2012
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 0.010 1.000 1 2012 2012
Renal carcinoma
CUI: C1378703
Disease: Renal carcinoma
21 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 0.010 1.000 1 2012 2012
Rheumatoid Nodule
CUI: C0035450
Disease: Rheumatoid Nodule
3 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 0.010 1.000 1 2010 2010
Superficial ulcer
CUI: C0333307
Disease: Superficial ulcer
10 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 0.010 1.000 1 2010 2010
Asthma
CUI: C0004096
Disease: Asthma
1536 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 0.020 1.000 2 2010 2012
Diffuse Large B-Cell Lymphoma
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
127 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 0.020 1.000 2 2009 2015
Myasthenia Gravis
CUI: C0026896
Disease: Myasthenia Gravis
93 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 0.020 0.500 2 2012 2018
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.752 0.400 16 27344882 missense variant A/C;G;T snv 0.45 0.020 1.000 2 2010 2014