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: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.010 1.000 1 2013 2013
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
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: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0271650
Disease: Impaired glucose tolerance
Impaired glucose tolerance 		Nutritional and Metabolic Diseases 0.010 1.000 1 2005 2005
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0520679
Disease: Sleep Apnea, Obstructive
Sleep Apnea, Obstructive 		Respiratory Tract Diseases; Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0577631
Disease: Carotid Atherosclerosis
Carotid Atherosclerosis 		Nervous System Diseases; Cardiovascular Diseases 0.010 1.000 1 2000 2000
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.010 < 0.001 1 2006 2006
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0003467
Disease: Anxiety
Anxiety 		Behavior and Behavior Mechanisms 0.010 1.000 1 2009 2009
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0342257
Disease: Complications of Diabetes Mellitus
Complications of Diabetes Mellitus 		Endocrine System Diseases 0.010 1.000 1 2007 2007
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0013473
Disease: Eating Disorders
Eating Disorders 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0042900
Disease: Vitiligo
Vitiligo 		Skin and Connective Tissue Diseases 0.010 1.000 1 2014 2014
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.010 < 0.001 1 2006 2006
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.010 1.000 1 2007 2007
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0022658
Disease: Kidney Diseases
Kidney Diseases 		Female Urogenital Diseases and Pregnancy Complications; Male Urogenital Diseases 0.010 1.000 1 2006 2006
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs16139
rs16139 		0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02
CUI: C0025517
Disease: Metabolic Diseases
Metabolic Diseases 		Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017
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: 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