Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis 		0.700 1.000 1 2013 2013
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.020 0.500 2 2010 2015
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.020 0.500 2 2010 2018
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.020 0.500 2 2010 2015
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.020 0.500 2 2010 2018
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis 		0.020 0.500 2 2010 2017
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0016053
Disease: Fibromyalgia
Fibromyalgia 		0.010 1.000 1 2015 2015
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0036690
Disease: Septicemia
Septicemia 		0.010 1.000 1 2013 2013
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0677659
Disease: Gastro-esophageal reflux disease with esophagitis
Gastro-esophageal reflux disease with esophagitis 		0.010 < 0.001 1 2008 2008
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0017154
Disease: Gastritis, Atrophic
Gastritis, Atrophic 		0.010 1.000 1 2008 2008
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0007102
Disease: Malignant tumor of colon
Malignant tumor of colon 		0.010 1.000 1 2012 2012
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0243026
Disease: Sepsis
Sepsis 		0.010 1.000 1 2013 2013
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0004763
Disease: Barrett Esophagus
Barrett Esophagus 		0.010 < 0.001 1 2008 2008
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0085695
Disease: Chronic gastritis
Chronic gastritis 		0.010 < 0.001 1 2010 2010
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis 		0.010 1.000 1 2013 2013
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia 		0.010 1.000 1 2010 2010
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C2937365
Disease: Recurrent aphthous ulcer
Recurrent aphthous ulcer 		0.010 1.000 1 2011 2011
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.010 1.000 1 2009 2009
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0014869
Disease: Peptic Esophagitis
Peptic Esophagitis 		0.010 < 0.001 1 2008 2008
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0279628
Disease: Adenocarcinoma Of Esophagus
Adenocarcinoma Of Esophagus 		0.010 1.000 1 2008 2008
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		0.010 1.000 1 2010 2010
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0036221
Disease: Mast-Cell Sarcoma
Mast-Cell Sarcoma 		0.010 1.000 1 2015 2015
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0024305
Disease: Lymphoma, Non-Hodgkin
Lymphoma, Non-Hodgkin 		0.010 1.000 1 2006 2006
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C1839735
Disease: MILES-CARPENTER X-LINKED MENTAL RETARDATION SYNDROME
MILES-CARPENTER X-LINKED MENTAL RETARDATION SYNDROME 		0.010 1.000 1 2015 2015
dbSNP: rs2297518
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2015 2015