rs1801274, FCGR2A

N. diseases: 46
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.
Adult Non-Hodgkin Lymphoma
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
39 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2006 2006
Childhood Non-Hodgkin Lymphoma
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
39 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2006 2006
Influenza
CUI: C0021400
Disease: Influenza
17 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2006 2006
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2006 2006
Lymphoma, Non-Hodgkin, Familial
CUI: C4721532
Disease: Lymphoma, Non-Hodgkin, Familial
79 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2006 2006
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2007 2007
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.810 1.000 5 2008 2017
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.850 1.000 9 2009 2018
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.040 1.000 4 2009 2019
Heparin-induced thrombocytopenia
CUI: C0272285
Disease: Heparin-induced thrombocytopenia
5 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2009 2009
Diabetes Mellitus, Insulin-Dependent
954 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2010 2010
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2010 2010
Mucocutaneous Lymph Node Syndrome
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
195 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.880 1.000 9 2011 2019
CATARACT, ANTERIOR POLAR
CUI: C1855179
Disease: CATARACT, ANTERIOR POLAR
27 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2011 2011
Community acquired pneumonia
CUI: C0694549
Disease: Community acquired pneumonia
13 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2011 2011
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
36 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2011 2011
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.800 1.000 3 2012 2017
Clinical malaria
CUI: C4543807
Disease: Clinical malaria
3 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2012 2012
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2012 2012
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.700 1.000 1 2012 2012
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2012 2012
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.700 1.000 1 2013 2013
Periodontitis
CUI: C0031099
Disease: Periodontitis
116 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2013 2013
Dengue Fever
CUI: C0011311
Disease: Dengue Fever
39 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.020 1.000 2 2014 2015
Asthma
CUI: C0004096
Disease: Asthma
1536 0.597 0.800 1 161509955 missense variant A/C;G snv 4.0E-06; 0.48 0.010 1.000 1 2014 2014