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: rs1799732
rs1799732 		0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.050 1.000 5 2007 2019
dbSNP: rs1076560
rs1076560 		0.776 0.120 11 113412966 intron variant C/A snv 0.16
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.040 1.000 4 2012 2017
dbSNP: rs1076560
rs1076560 		0.776 0.120 11 113412966 intron variant C/A snv 0.16
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.020 1.000 2 2007 2014
dbSNP: rs1076560
rs1076560 		0.776 0.120 11 113412966 intron variant C/A snv 0.16
CUI: C0009171
Disease: Cocaine Abuse
Cocaine Abuse 		Chemically-Induced Disorders; Mental Disorders 0.020 1.000 2 2011 2014
dbSNP: rs1076560
rs1076560 		0.776 0.120 11 113412966 intron variant C/A snv 0.16
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis 		Mental Disorders 0.020 0.500 2 2015 2019
dbSNP: rs1076560
rs1076560 		0.776 0.120 11 113412966 intron variant C/A snv 0.16
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.020 1.000 2 2016 2018
dbSNP: rs1076560
rs1076560 		0.776 0.120 11 113412966 intron variant C/A snv 0.16
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		Mental Disorders 0.020 0.500 2 2015 2019
dbSNP: rs1079597
rs1079597 		0.827 0.080 11 113425564 intron variant C/T snv 0.18
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence 		Chemically-Induced Disorders; Mental Disorders 0.020 1.000 2 2013 2019
dbSNP: rs1079597
rs1079597 		0.827 0.080 11 113425564 intron variant C/T snv 0.18
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		Chemically-Induced Disorders; Mental Disorders 0.020 1.000 2 2014 2017
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: 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: 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
dbSNP: rs1076562
rs1076562 		0.925 0.120 11 113425286 intron variant A/G snv 0.65
CUI: C1861537
Disease: OROFACIAL CLEFT 1
OROFACIAL CLEFT 1 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases; Stomatognathic Diseases 0.010 1.000 1 2011 2011
dbSNP: rs1079596
rs1079596 		11 113425897 intron variant C/A;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1079597
rs1079597 		0.827 0.080 11 113425564 intron variant C/T snv 0.18
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs1079597
rs1079597 		0.827 0.080 11 113425564 intron variant C/T snv 0.18
CUI: C0600427
Disease: Cocaine Dependence
Cocaine Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs1079597
rs1079597 		0.827 0.080 11 113425564 intron variant C/T snv 0.18
CUI: C0028043
Disease: Nicotine Dependence
Nicotine Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2015 2015
dbSNP: rs1110976
rs1110976 		1.000 0.040 11 113413797 intron variant T/G snv
CUI: C0003467
Disease: Anxiety
Anxiety 		Behavior and Behavior Mechanisms 0.010 1.000 1 2008 2008
dbSNP: rs1110976
rs1110976 		1.000 0.040 11 113413797 intron variant T/G snv
CUI: C0236734
Disease: Caffeine related disorders
Caffeine related disorders 		0.010 1.000 1 2008 2008