NPY, neuropeptide Y, 4852

N. diseases: 381; N. variants: 12
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.040 1.000 4 2012 2015
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.020 1.000 2 2015 2016
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.020 0.500 2 2014 2015
dbSNP: rs17149106
rs17149106 		0.925 0.160 7 24283588 upstream gene variant G/T snv
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.020 1.000 2 2011 2016
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C1533217
Disease: Methamphetamine dependence
Methamphetamine dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2012 2012
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C0042900
Disease: Vitiligo
Vitiligo 		Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2010 2010
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C0040332
Disease: Tobacco Dependence
Tobacco Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C0270549
Disease: Generalized Anxiety Disorder
Generalized Anxiety Disorder 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis 		Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding) 		Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2015 2015
dbSNP: rs16147
rs16147 		0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs16148
rs16148 		7 24282719 upstream gene variant T/C snv 0.42
CUI: C0042571
Disease: Vertigo
Vertigo 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Otorhinolaryngologic Diseases 0.010 1.000 1 2018 2018
dbSNP: rs17149106
rs17149106 		0.925 0.160 7 24283588 upstream gene variant G/T snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs16475
rs16475 		0.925 0.120 7 24291867 downstream gene variant A/G snv 5.3E-02
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs16475
rs16475 		0.925 0.120 7 24291867 downstream gene variant A/G snv 5.3E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2013 2013