DRD2, dopamine receptor D2, 1813

N. diseases: 437; N. variants: 42
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: rs1079727
rs1079727 		1.000 0.040 11 113418460 intron variant T/C snv 0.16
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.020 1.000 2 2013 2014
dbSNP: rs1799732
rs1799732 		0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.020 0.500 2 2013 2015
dbSNP: rs1801028
rs1801028 		0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0011253
Disease: Delusions
Delusions 		Behavior and Behavior Mechanisms 0.020 1.000 2 1996 2000
dbSNP: rs1801028
rs1801028 		0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0004936
Disease: Mental disorders
Mental disorders 		Mental Disorders 0.020 1.000 2 1996 2010
dbSNP: rs1801028
rs1801028 		0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		Mental Disorders 0.020 0.500 2 1998 2000
dbSNP: rs1801028
rs1801028 		0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.020 1.000 2 1995 2003
dbSNP: rs2283265
rs2283265 		0.776 0.160 11 113414814 intron variant C/A snv 0.16
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.020 1.000 2 2013 2014
dbSNP: rs6277
rs6277 		0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.020 0.500 2 2008 2013
dbSNP: rs6277
rs6277 		0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
Drug-induced tardive dyskinesia 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Chemically-Induced Disorders 0.020 1.000 2 2007 2013
dbSNP: rs6277
rs6277 		0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38
CUI: C0038506
Disease: Stuttering
Stuttering 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.020 1.000 2 2012 2019
dbSNP: rs6277
rs6277 		0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.020 1.000 2 2014 2019
dbSNP: rs6277
rs6277 		0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38
CUI: C0028043
Disease: Nicotine Dependence
Nicotine Dependence 		Chemically-Induced Disorders; Mental Disorders 0.020 1.000 2 2012 2017
dbSNP: rs6277
rs6277 		0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior 		Behavior and Behavior Mechanisms 0.020 1.000 2 2009 2010
dbSNP: rs6277
rs6277 		0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38
CUI: C4694057
Disease: Taq1A POLYMORPHISM
Taq1A POLYMORPHISM 		0.020 1.000 2 2009 2019
dbSNP: rs6277
rs6277 		0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.020 1.000 2 2007 2013
dbSNP: rs6277
rs6277 		0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.020 1.000 2 2014 2018
dbSNP: rs767413934
rs767413934 		0.925 0.120 11 113424539 missense variant G/A snv 4.0E-06
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.020 1.000 2 2008 2008
dbSNP: rs767413934
rs767413934 		0.925 0.120 11 113424539 missense variant G/A snv 4.0E-06
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
Drug-induced tardive dyskinesia 		Pathological Conditions, Signs and Symptoms; Nervous System Diseases; Chemically-Induced Disorders 0.020 1.000 2 2008 2008
dbSNP: rs104894220
rs104894220 		1.000 0.040 11 113416935 missense variant C/T snv 4.4E-05 6.3E-05
CUI: C1834570
Disease: Myoclonic dystonia
Myoclonic dystonia 		Nervous System Diseases 0.010 1.000 1 2000 2000
dbSNP: rs1076560
rs1076560 		0.776 0.120 11 113412966 intron variant C/A snv 0.16
CUI: C0038586
Disease: Substance Use Disorders
Substance Use Disorders 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs1076560
rs1076560 		0.776 0.120 11 113412966 intron variant C/A snv 0.16
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs1076560
rs1076560 		0.776 0.120 11 113412966 intron variant C/A snv 0.16
CUI: C3160814
Disease: Cannabis use
Cannabis use 		0.010 1.000 1 2015 2015
dbSNP: rs1076560
rs1076560 		0.776 0.120 11 113412966 intron variant C/A snv 0.16
CUI: C1510472
Disease: Drug Dependence
Drug Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs1076560
rs1076560 		0.776 0.120 11 113412966 intron variant C/A snv 0.16
CUI: C0524662
Disease: Opiate Addiction
Opiate Addiction 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs1076562
rs1076562 		0.925 0.120 11 113425286 intron variant A/G snv 0.65
CUI: C3714941
Disease: OTOFACIOCERVICAL SYNDROME 1
OTOFACIOCERVICAL SYNDROME 1 		0.010 1.000 1 2011 2011