ARVCF, ARVCF delta catenin family member, 421

N. diseases: 151; N. variants: 30
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: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.100 0.727 11 2004 2018
dbSNP: rs165815
rs165815 		0.882 0.120 22 19971950 missense variant C/T snv 0.75 0.72
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.020 0.500 2 2005 2010
dbSNP: rs165655
rs165655 		1.000 0.040 22 19970240 3 prime UTR variant G/A snv 0.56
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2005 2005
dbSNP: rs749437638
rs749437638 		0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		Immune System Diseases; Nervous System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs749437638
rs749437638 		0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05
CUI: C0042373
Disease: Vascular Diseases
Vascular Diseases 		Cardiovascular Diseases 0.010 1.000 1 2006 2006
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases 0.010 1.000 1 2007 2007
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0006012
Disease: Borderline Personality Disorder
Borderline Personality Disorder 		Mental Disorders 0.010 1.000 1 2007 2007
dbSNP: rs749437638
rs749437638 		0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.050 1.000 5 2008 2017
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0028768
Disease: Obsessive-Compulsive Disorder
Obsessive-Compulsive Disorder 		Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs749437638
rs749437638 		0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs749437638
rs749437638 		0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05
CUI: C0011570
Disease: Mental Depression
Mental Depression 		Behavior and Behavior Mechanisms 0.010 1.000 1 2008 2008
dbSNP: rs749437638
rs749437638 		0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05
CUI: C0344315
Disease: Depressed mood
Depressed mood 		Behavior and Behavior Mechanisms 0.010 1.000 1 2008 2008
dbSNP: rs165849
rs165849 		1.000 0.040 22 19971146 intron variant G/A snv 0.55
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.020 1.000 2 2009 2009
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0011253
Disease: Delusions
Delusions 		Behavior and Behavior Mechanisms 0.010 1.000 1 2009 2009
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0018524
Disease: Hallucinations
Hallucinations 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Behavior and Behavior Mechanisms 0.010 1.000 1 2009 2009
dbSNP: rs2239395
rs2239395 		1.000 0.040 22 19974680 intron variant T/G snv 0.13
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs2518823
rs2518823 		1.000 0.040 22 19972665 intron variant T/C snv 0.86
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs887199
rs887199 		1.000 0.040 22 19974432 intron variant A/G snv 0.72
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.030 1.000 3 2010 2020
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		Behavior and Behavior Mechanisms 0.010 1.000 1 2010 2010
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2010 2010
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0004936
Disease: Mental disorders
Mental disorders 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
Drug-induced tardive dyskinesia 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Chemically-Induced Disorders 0.010 1.000 1 2010 2010
dbSNP: rs165815
rs165815 		0.882 0.120 22 19971950 missense variant C/T snv 0.75 0.72
CUI: C0809983
Disease: Schizophrenia and related disorders
Schizophrenia and related disorders 		Mental Disorders 0.010 1.000 1 2010 2010