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.
Acquired aplastic anemia
CUI: C0271907
Disease: Acquired aplastic anemia
12 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2016 2016
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
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
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
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
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.050 0.800 5 2007 2015
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
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.080 1.000 8 2006 2015
Carcinoma, Ovarian Epithelial
CUI: C4721610
Disease: Carcinoma, Ovarian Epithelial
327 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.020 1.000 2 2001 2019
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
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
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.070 0.714 7 2005 2013
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
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.050 0.600 5 2013 2015
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.050 0.600 5 2013 2015
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
Head and Neck Carcinoma
CUI: C3887461
Disease: Head and Neck Carcinoma
118 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.030 1.000 3 2003 2015