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: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		0.010 1.000 1 1996 1996
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0001723
Disease: Affective Disorders, Psychotic
Affective Disorders, Psychotic 		0.010 1.000 1 1996 1996
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0018524
Disease: Hallucinations
Hallucinations 		0.010 1.000 1 1996 1996
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.010 1.000 1 1996 1996
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.030 0.667 3 1996 1998
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis 		0.010 1.000 1 1998 1998
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0740858
Disease: Substance abuse problem
Substance abuse problem 		0.010 1.000 1 1998 1998
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0011253
Disease: Delusions
Delusions 		0.020 1.000 2 1996 2000
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders 		0.020 0.500 2 1998 2000
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
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0024517
Disease: Major depression, single episode
Major depression, single episode 		0.010 1.000 1 2001 2001
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0011251
Disease: Delusional disorder
Delusional disorder 		0.010 1.000 1 2002 2002
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.020 1.000 2 1995 2003
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0027849
Disease: Neuroleptic Malignant Syndrome
Neuroleptic Malignant Syndrome 		0.010 1.000 1 2004 2004
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0871099
Disease: positive and negative symptoms
positive and negative symptoms 		0.010 1.000 1 2004 2004
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia 		0.030 1.000 3 2001 2005
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
Drug-induced tardive dyskinesia 		0.030 1.000 3 2001 2005
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0085602
Disease: Polydipsia
Polydipsia 		0.010 1.000 1 2005 2005
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C0525041
Disease: Neurobehavioral Manifestations
Neurobehavioral Manifestations 		0.010 1.000 1 2005 2005
dbSNP: rs1801028
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02
CUI: C1263846
Disease: Attention deficit hyperactivity disorder
Attention deficit hyperactivity disorder 		0.010 1.000 1 2005 2005
dbSNP: rs6277
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38
CUI: C0221271
Disease: Elastosis perforans serpiginosa
Elastosis perforans serpiginosa 		0.010 1.000 1 2006 2006
dbSNP: rs6277
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38
CUI: C1868684
Disease: EAR, PATELLA, SHORT STATURE SYNDROME
EAR, PATELLA, SHORT STATURE SYNDROME 		0.010 1.000 1 2006 2006
dbSNP: rs147347002
rs147347002
DRD2
1.000 11 113416879 synonymous variant G/A snv 1.9E-04 6.6E-04
CUI: C4694057
Disease: Taq1A POLYMORPHISM
Taq1A POLYMORPHISM 		0.010 1.000 1 2007 2007
dbSNP: rs6275
rs6275
DRD2
0.851 0.160 11 113412755 synonymous variant A/G snv 0.64 0.58
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia 		0.010 < 0.001 1 2007 2007
dbSNP: rs6275
rs6275
DRD2
0.851 0.160 11 113412755 synonymous variant A/G snv 0.64 0.58
CUI: C3714760
Disease: Drug-induced tardive dyskinesia
Drug-induced tardive dyskinesia 		0.010 < 0.001 1 2007 2007