Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.050 1.000 5 2007 2019
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.020 0.500 2 2013 2015
dbSNP: rs767413934
rs767413934
DRD2
0.925 0.120 11 113424539 missense variant G/A snv 4.0E-06
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia 		0.020 1.000 2 2008 2008
dbSNP: rs767413934
rs767413934
DRD2
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 		0.020 1.000 2 2008 2008
dbSNP: rs1079596
rs1079596
DRD2
11 113425897 intron variant C/A;T snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.700 1.000 1 2018 2018
dbSNP: rs1110976
rs1110976
DRD2
1.000 0.040 11 113413797 intron variant T/G snv
CUI: C0003467
Disease: Anxiety
Anxiety 		0.010 1.000 1 2008 2008
dbSNP: rs1110976
rs1110976
DRD2
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
dbSNP: rs1110976
rs1110976
DRD2
1.000 0.040 11 113413797 intron variant T/G snv
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		0.010 1.000 1 2008 2008
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0027651
Disease: Neoplasms
Neoplasms 		0.010 1.000 1 2018 2018
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0524662
Disease: Opiate Addiction
Opiate Addiction 		0.010 1.000 1 2011 2011
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0001430
Disease: Adenoma
Adenoma 		0.010 1.000 1 2009 2009
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior 		0.010 1.000 1 2014 2014
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 1.000 1 2013 2013
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 2016 2016
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 2016 2016
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0038587
Disease: Substance Withdrawal Syndrome
Substance Withdrawal Syndrome 		0.010 1.000 1 2012 2012
dbSNP: rs1799732
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2016 2016
dbSNP: rs2734839
rs2734839
DRD2
1.000 0.040 11 113415768 intron variant C/A;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2012 2012
dbSNP: rs2734839
rs2734839
DRD2
1.000 0.040 11 113415768 intron variant C/A;T snv
CUI: C0582591
Disease: Processing speed
Processing speed 		0.700 1.000 1 2016 2016
dbSNP: rs2734841
rs2734841
DRD2
1.000 0.040 11 113411054 intron variant A/C;G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2013 2013
dbSNP: rs4648319
rs4648319
DRD2
1.000 0.080 11 113443641 intron variant G/A;T snv
CUI: C0019337
Disease: Heroin Dependence
Heroin Dependence 		0.010 1.000 1 2019 2019
dbSNP: rs7131627
rs7131627
DRD2
11 113429107 intron variant G/A;C snv
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.700 1.000 1 2018 2018
dbSNP: rs1110977
rs1110977
DRD2
1.000 0.040 11 113412643 missense variant T/A;C snv 7.0E-06
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2013 2013
dbSNP: rs1334465665
rs1334465665
DRD2
1.000 0.080 11 113414400 missense variant C/T snv 2.1E-05
CUI: C0028043
Disease: Nicotine Dependence
Nicotine Dependence 		0.010 1.000 1 2011 2011
dbSNP: rs104894220
rs104894220
DRD2
1.000 0.040 11 113416935 missense variant C/T snv 4.4E-05 6.3E-05
CUI: C1834570
Disease: Myoclonic dystonia
Myoclonic dystonia 		0.010 1.000 1 2000 2000