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.
CANCER PROGRESSION AND TUMOR CELL MOTILITY
CUI: C4016099
Disease: CANCER PROGRESSION AND TUMOR CELL MOTILITY
1 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.700 0
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2005 2005
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2005 2005
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2006 2006
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2006 2006
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2006 2006
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
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2008 2008
Progression of prostate cancer
CUI: C1739135
Disease: Progression of prostate cancer
7 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 0.010 1.000 1 2008 2008
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
Pituitary-dependent Cushing's disease
CUI: C0221406
Disease: 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
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
CUI: C1262211
Disease: 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
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
CUI: C1337011
Disease: 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
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