FAAH, fatty acid amide hydrolase, 2166

N. diseases: 177; N. variants: 8
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: rs11576941
rs11576941 		1 46409395 intron variant G/T snv 0.27
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure 		0.700 1.000 1 2019 2019
dbSNP: rs772931153
rs772931153 		1.000 0.080 1 46408541 missense variant C/A snv 4.0E-06
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		Neoplasms; Skin and Connective Tissue Diseases 0.700 0
dbSNP: rs324420
rs324420 		0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.090 0.889 9 2008 2020
dbSNP: rs324420
rs324420 		0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26
CUI: C0085281
Disease: Addictive Behavior
Addictive Behavior 		Behavior and Behavior Mechanisms 0.050 1.000 5 2004 2020
dbSNP: rs324420
rs324420 		0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26
CUI: C1561826
Disease: Overweight and obesity
Overweight and obesity 		0.050 1.000 5 2007 2013
dbSNP: rs324420
rs324420 		0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26
CUI: C0242510
Disease: Drug usage
Drug usage 		Chemically-Induced Disorders; Mental Disorders 0.040 1.000 4 2004 2010
dbSNP: rs324420
rs324420 		0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26
CUI: C0024809
Disease: Marijuana Abuse
Marijuana Abuse 		Chemically-Induced Disorders; Mental Disorders 0.030 0.667 3 2007 2009
dbSNP: rs324420
rs324420 		0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		Mental Disorders 0.030 1.000 3 2015 2016
dbSNP: rs324420
rs324420 		0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.020 1.000 2 2014 2016
dbSNP: rs324420
rs324420 		0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.020 1.000 2 2008 2009
dbSNP: rs324420
rs324420 		0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26
CUI: C0028756
Disease: Obesity, Morbid
Obesity, Morbid 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.020 0.500 2 2008 2015
dbSNP: rs324420
rs324420 		0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26
CUI: C1533217
Disease: Methamphetamine dependence
Methamphetamine dependence 		Chemically-Induced Disorders; Mental Disorders 0.020 1.000 2 2005 2013
dbSNP: rs324420
rs324420 		0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26
CUI: C1510472
Disease: Drug Dependence
Drug Dependence 		Chemically-Induced Disorders; Mental Disorders 0.020 1.000 2 2006 2014
dbSNP: rs324420
rs324420 		0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26
CUI: C0022104
Disease: Irritable Bowel Syndrome
Irritable Bowel Syndrome 		Digestive System Diseases 0.020 0.500 2 2011 2014
dbSNP: rs324420
rs324420 		0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26
CUI: C0563625
Disease: Agnosia for Pain
Agnosia for Pain 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms 0.020 1.000 2 2014 2016
dbSNP: rs324420
rs324420 		0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26
CUI: C0740858
Disease: Substance abuse problem
Substance abuse problem 		Chemically-Induced Disorders; Mental Disorders 0.020 1.000 2 2007 2008
dbSNP: rs2295632
rs2295632 		1.000 0.080 1 46413890 downstream gene variant T/G snv 0.60
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 < 0.001 1 2010 2010
dbSNP: rs2295633
rs2295633 		0.827 0.120 1 46408711 intron variant A/G;T snv
CUI: C0024809
Disease: Marijuana Abuse
Marijuana Abuse 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs2295633
rs2295633 		0.827 0.120 1 46408711 intron variant A/G;T snv
CUI: C0015672
Disease: Fatigue
Fatigue 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2010 2010
dbSNP: rs2295633
rs2295633 		0.827 0.120 1 46408711 intron variant A/G;T snv
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 1.000 1 2020 2020
dbSNP: rs2295633
rs2295633 		0.827 0.120 1 46408711 intron variant A/G;T snv
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
Post-Traumatic Stress Disorder 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs2295633
rs2295633 		0.827 0.120 1 46408711 intron variant A/G;T snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs2295633
rs2295633 		0.827 0.120 1 46408711 intron variant A/G;T snv
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2012 2012
dbSNP: rs2295633
rs2295633 		0.827 0.120 1 46408711 intron variant A/G;T snv
CUI: C3160814
Disease: Cannabis use
Cannabis use 		0.010 1.000 1 2019 2019
dbSNP: rs324419
rs324419 		0.925 0.120 1 46406314 stop gained T/A;C snv 0.87
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2012 2012