rs2234922, EPHX1

N. diseases: 42
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.
Malignant neoplasm of esophagus
CUI: C0546837
Disease: Malignant neoplasm of esophagus
214 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.070 0.571 7 2010 2015
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.060 0.667 6 2005 2013
Esophageal carcinoma
CUI: C0152018
Disease: Esophageal carcinoma
272 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.060 0.500 6 2010 2015
Esophageal Neoplasms
CUI: C0014859
Disease: Esophageal Neoplasms
270 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.060 0.500 6 2010 2015
Carcinoma of lung
CUI: C0684249
Disease: Carcinoma of lung
1204 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.050 1.000 5 2006 2015
Malignant neoplasm of lung
CUI: C0242379
Disease: Malignant neoplasm of lung
1142 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.050 1.000 5 2006 2015
Primary malignant neoplasm of lung
CUI: C1306460
Disease: Primary malignant neoplasm of lung
981 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.050 1.000 5 2006 2015
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.030 0.667 3 2011 2015
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.030 0.333 3 2005 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.030 0.333 3 2005 2014
Squamous cell carcinoma of esophagus
CUI: C0279626
Disease: Squamous cell carcinoma of esophagus
329 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.030 1.000 3 2006 2019
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.020 1.000 2 2007 2011
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.020 1.000 2 2004 2007
Head and Neck Carcinoma
CUI: C3887461
Disease: Head and Neck Carcinoma
118 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.020 1.000 2 2003 2015
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.020 1.000 2 2013 2014
Malignant Head and Neck Neoplasm
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
118 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.020 1.000 2 2003 2015
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.020 1.000 2 2011 2014
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.020 1.000 2 2011 2013
Acquired aplastic anemia
CUI: C0271907
Disease: Acquired aplastic anemia
12 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.010 1.000 1 2016 2016
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
213 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.010 1.000 1 2012 2012
Adult Diffuse Large B-Cell Lymphoma
CUI: C1332201
Disease: Adult Diffuse Large B-Cell Lymphoma
46 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.010 1.000 1 2011 2011
Asthma
CUI: C0004096
Disease: Asthma
1536 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.010 1.000 1 2011 2011
Bladder Neoplasm
CUI: C0005695
Disease: Bladder Neoplasm
281 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.010 1.000 1 2011 2011
Brain Neoplasms
CUI: C0006118
Disease: Brain Neoplasms
204 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.010 1.000 1 2013 2013
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.010 1.000 1 2011 2011