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: rs165849
rs165849 		1.000 0.040 22 19971146 intron variant G/A snv 0.55
CUI: C0809983
Disease: Schizophrenia and related disorders
Schizophrenia and related disorders 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs35219372
rs35219372 		22 19971288 synonymous variant C/A;G;T snv 6.1E-06; 6.1E-06; 1.7E-02
CUI: C0809983
Disease: Schizophrenia and related disorders
Schizophrenia and related disorders 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs5993890
rs5993890 		22 19971306 synonymous variant G/A;C snv 6.7E-02; 1.2E-05
CUI: C0809983
Disease: Schizophrenia and related disorders
Schizophrenia and related disorders 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs9332377
rs9332377 		0.882 0.120 22 19968169 intron variant C/A;T snv
CUI: C0028043
Disease: Nicotine Dependence
Nicotine Dependence 		Chemically-Induced 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: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.020 1.000 2 2011 2012
dbSNP: rs1034566
rs1034566 		22 19996754 intron variant C/G;T snv
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement 		0.800 1.000 1 2011 2011
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0438696
Disease: Suicidal
Suicidal 		Behavior and Behavior Mechanisms 0.010 1.000 1 2011 2011
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs2073746
rs2073746 		1.000 0.080 22 19991035 intron variant T/C snv 0.80
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction 		Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases 0.700 1.000 1 2011 2011
dbSNP: rs749437638
rs749437638 		0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05
CUI: C0080178
Disease: Spina Bifida
Spina Bifida 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.010 1.000 1 2011 2011
dbSNP: rs9332377
rs9332377 		0.882 0.120 22 19968169 intron variant C/A;T snv
CUI: C0438696
Disease: Suicidal
Suicidal 		Behavior and Behavior Mechanisms 0.010 1.000 1 2011 2011
dbSNP: rs749437638
rs749437638 		0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.020 1.000 2 2012 2015
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0338831
Disease: Manic
Manic 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C0853193
Disease: Bipolar I disorder
Bipolar I disorder 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs174697
rs174697 		0.851 0.080 22 19966309 intron variant A/G snv 0.88
CUI: C0011570
Disease: Mental Depression
Mental Depression 		Behavior and Behavior Mechanisms 0.010 1.000 1 2012 2012
dbSNP: rs174697
rs174697 		0.851 0.080 22 19966309 intron variant A/G snv 0.88
CUI: C0344315
Disease: Depressed mood
Depressed mood 		Behavior and Behavior Mechanisms 0.010 1.000 1 2012 2012
dbSNP: rs174697
rs174697 		0.851 0.080 22 19966309 intron variant A/G snv 0.88
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs174697
rs174697 		0.851 0.080 22 19966309 intron variant A/G snv 0.88
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs174697
rs174697 		0.851 0.080 22 19966309 intron variant A/G snv 0.88
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		Mental Disorders 0.010 1.000 1 2012 2012
dbSNP: rs5993889
rs5993889 		22 19967852 intron variant T/C;G snv
CUI: C0428472
Disease: Serum HDL cholesterol measurement
Serum HDL cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs5993889
rs5993889 		22 19967852 intron variant T/C;G snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.700 1.000 1 2012 2012
dbSNP: rs165599
rs165599 		0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 1.000 1 2013 2013
dbSNP: rs887200
rs887200 		22 19976143 intron variant C/T snv 0.74
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2013 2013