rs2297518, NOS2

N. diseases: 30
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.
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.700 1.000 1 2013 2013
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.020 0.500 2 2010 2017
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.020 0.500 2 2010 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.020 0.500 2 2010 2015
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.020 0.500 2 2010 2015
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.020 0.500 2 2010 2018
Adenocarcinoma Of Esophagus
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
81 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1.000 1 2008 2008
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
60 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1 2008 2008
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1.000 1 2010 2010
Chronic gastritis
CUI: C0085695
Disease: Chronic gastritis
11 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1 2010 2010
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1.000 1 2012 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1.000 1 2010 2010
Fibromyalgia
CUI: C0016053
Disease: Fibromyalgia
38 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1.000 1 2015 2015
Gastritis, Atrophic
CUI: C0017154
Disease: Gastritis, Atrophic
61 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1.000 1 2008 2008
Gastro-esophageal reflux disease with esophagitis
3 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1 2008 2008
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1.000 1 2015 2015
Infection caused by Helicobacter pylori
56 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1.000 1 2010 2010
Liver Cirrhosis
CUI: C0023890
Disease: Liver Cirrhosis
189 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1.000 1 2013 2013
Lymphoma, Non-Hodgkin
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
197 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1.000 1 2006 2006
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1.000 1 2009 2009
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1.000 1 2012 2012
Mast-Cell Sarcoma
CUI: C0036221
Disease: Mast-Cell Sarcoma
4 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1.000 1 2015 2015
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1.000 1 2012 2012
MILES-CARPENTER X-LINKED MENTAL RETARDATION SYNDROME
2 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1.000 1 2015 2015
Peptic Esophagitis
CUI: C0014869
Disease: Peptic Esophagitis
3 0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 0.010 1 2008 2008