rs351855, FGFR4

N. diseases: 58
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.
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.020 1.000 2 2012 2014
Febrile Neutropenia
CUI: C0746883
Disease: Febrile Neutropenia
14 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2014 2014
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2014 2014
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.040 0.500 4 2010 2013
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.020 0.500 2 2010 2013
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.020 0.500 2 2010 2013
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2013 2013
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2013 2013
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2013 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.020 1.000 2 2012 2012
Cholelithiasis
CUI: C0008350
Disease: Cholelithiasis
90 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2012 2012
Head and Neck Carcinoma
CUI: C3887461
Disease: Head and Neck Carcinoma
118 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2012 2012
Islet Cell Tumor
CUI: C0242363
Disease: Islet Cell Tumor
5 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2012 2012
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
118 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2012 2012
Oropharynx (excludes nasopharynx)
CUI: C0549523
Disease: Oropharynx (excludes nasopharynx)
5 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2012 2012
Sarcoma
CUI: C1261473
Disease: Sarcoma
42 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2012 2012
Sarcoma of soft tissue
CUI: C4551687
Disease: Sarcoma of soft tissue
6 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2012 2012
Squamous cell carcinoma of mouth
CUI: C0585362
Disease: Squamous cell carcinoma of mouth
1 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2012 2012
Well Differentiated Pancreatic Endocrine Tumor
3 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2012 2012
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2011 2011
Diarrhoea predominant irritable bowel syndrome
8 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2011 2011
Eclampsia
CUI: C0013537
Disease: Eclampsia
38 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1 2011 2011
Pituitary-dependent Cushing's disease
8 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2010 2010
Adenocarcinoma of lung (disorder)
CUI: C0152013
Disease: Adenocarcinoma of lung (disorder)
563 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.020 1.000 2 2005 2009
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2008 2008