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.
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
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
441 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2013 2013
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
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
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2017 2017
Congenital Abnormality
CUI: C0000768
Disease: Congenital Abnormality
73 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2019 2019
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
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2014 2014
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
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
Influenza-like illness
CUI: C0521839
Disease: Influenza-like illness
3 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2016 2016
Influenza-like symptoms
CUI: C0392171
Disease: Influenza-like symptoms
4 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2016 2016
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
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2018 2018
Malignant neoplasm of skin
CUI: C0007114
Disease: Malignant neoplasm of skin
38 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2015 2015
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
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
Medulloblastoma
CUI: C0025149
Disease: Medulloblastoma
115 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2012 2012
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
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