IFNGR2, interferon gamma receptor 2, 3460

N. diseases: 71; N. variants: 13
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs74315444
rs74315444 		1.000 21 33426974 missense variant C/A snv
CUI: C0026918
Disease: Mycobacterium Infections
Mycobacterium Infections 		Infections 0.010 1.000 1 2019 2019
dbSNP: rs8126756
rs8126756 		0.925 0.040 21 33403138 5 prime UTR variant T/C;G snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs8126756
rs8126756 		0.925 0.040 21 33403138 5 prime UTR variant T/C;G snv
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		Digestive System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs8126756
rs8126756 		0.925 0.040 21 33403138 5 prime UTR variant T/C;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.010 1.000 1 2018 2018
dbSNP: rs9808753
rs9808753 		0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C0155877
Disease: Allergic asthma
Allergic asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2001 2001
dbSNP: rs9808753
rs9808753 		0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C0242647
Disease: Mucosa-Associated Lymphoid Tissue Lymphoma
Mucosa-Associated Lymphoid Tissue Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs9808753
rs9808753 		0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.010 1.000 1 2014 2014
dbSNP: rs9808753
rs9808753 		0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C0151517
Disease: Complete atrioventricular block
Complete atrioventricular block 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.010 1.000 1 2014 2014
dbSNP: rs9808753
rs9808753 		0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C0079731
Disease: B-Cell Lymphomas
B-Cell Lymphomas 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs9808753
rs9808753 		0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C0079772
Disease: T-Cell Lymphoma
T-Cell Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs9808753
rs9808753 		0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C1827849
Disease: IgE-mediated allergic asthma
IgE-mediated allergic asthma 		Immune System Diseases 0.010 1.000 1 2001 2001
dbSNP: rs9808753
rs9808753 		0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs9808753
rs9808753 		0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs9808753
rs9808753 		0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C0024301
Disease: Lymphoma, Follicular
Lymphoma, Follicular 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs9808753
rs9808753 		0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C1367654
Disease: Marginal Zone B-Cell Lymphoma
Marginal Zone B-Cell Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs9808753
rs9808753 		0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C0855095
Disease: Small Lymphocytic Lymphoma
Small Lymphocytic Lymphoma 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs9808753
rs9808753 		0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C0023434
Disease: Chronic Lymphocytic Leukemia
Chronic Lymphocytic Leukemia 		Neoplasms; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs9808753
rs9808753 		0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2005 2005
dbSNP: rs9808753
rs9808753 		0.701 0.400 21 33415005 missense variant A/G snv 0.20 0.18
CUI: C0042749
Disease: Viremia
Viremia 		Pathological Conditions, Signs and Symptoms; Infections 0.010 1.000 1 2011 2011