rs1051740, EPHX1

N. diseases: 56
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.
Polyp of large intestine
CUI: C0949059
Disease: Polyp of large intestine
32 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2001 2001
Squamous cell carcinoma of the head and neck
CUI: C1168401
Disease: Squamous cell carcinoma of the head and neck
348 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2003 2003
Age related macular degeneration
CUI: C0242383
Disease: Age related macular degeneration
663 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2005 2005
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2006 2006
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2006 2006
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.020 1.000 2 2007 2008
Pancreatic Diseases
CUI: C0030286
Disease: Pancreatic Diseases
11 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2009 2009
Pancreatitis
CUI: C0030305
Disease: Pancreatitis
80 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1 2009 2009
Craniofacial Abnormalities
CUI: C0376634
Disease: Craniofacial Abnormalities
4 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2010 2010
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.020 1.000 2 2007 2011
Asthma
CUI: C0004096
Disease: Asthma
1536 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.020 1.000 2 2009 2011
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2011 2011
Bulla of lung
CUI: C0241982
Disease: Bulla of lung
2 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2011 2011
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2011 2011
Carcinoma of bladder
CUI: C0699885
Disease: Carcinoma of bladder
309 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2011 2011
Hyperplastic Polyp
CUI: C0333983
Disease: Hyperplastic Polyp
22 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2011 2011
Laryngeal Diseases
CUI: C0023051
Disease: Laryngeal Diseases
7 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2011 2011
Malignant neoplasm of urinary bladder
CUI: C0005684
Disease: Malignant neoplasm of urinary bladder
316 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2011 2011
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2011 2011
Wheezing
CUI: C0043144
Disease: Wheezing
54 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2011 2011
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1 2012 2012
Adult Medulloblastoma
CUI: C0278876
Disease: Adult Medulloblastoma
24 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2012 2012
Childhood Acute Lymphoblastic Leukemia
CUI: C0023452
Disease: Childhood Acute Lymphoblastic Leukemia
261 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2012 2012
Childhood Medulloblastoma
CUI: C0278510
Disease: Childhood Medulloblastoma
25 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2012 2012
Familial lichen amyloidosis
CUI: C0268398
Disease: Familial lichen amyloidosis
24 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2012 2012