HTR1A, 5-hydroxytryptamine receptor 1A, 3350

N. diseases: 229; N. variants: 9
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: rs1800041
rs1800041 		0.882 0.120 5 63961673 missense variant G/A snv 1.8E-03 5.3E-04
CUI: C0344315
Disease: Depressed mood
Depressed mood 		Behavior and Behavior Mechanisms 0.010 1.000 1 2004 2004
dbSNP: rs1800041
rs1800041 		0.882 0.120 5 63961673 missense variant G/A snv 1.8E-03 5.3E-04
CUI: C0011570
Disease: Mental Depression
Mental Depression 		Behavior and Behavior Mechanisms 0.010 1.000 1 2004 2004
dbSNP: rs1800042
rs1800042 		1.000 0.040 5 63960902 missense variant C/A;T snv 8.0E-06; 1.4E-03
CUI: C0852733
Disease: Completed Suicide
Completed Suicide 		0.010 1.000 1 2002 2002
dbSNP: rs1800042
rs1800042 		1.000 0.040 5 63960902 missense variant C/A;T snv 8.0E-06; 1.4E-03
CUI: C0028768
Disease: Obsessive-Compulsive Disorder
Obsessive-Compulsive Disorder 		Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs1800044
rs1800044 		0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		Mental Disorders 0.010 1.000 1 1998 1998
dbSNP: rs1800044
rs1800044 		0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		Behavior and Behavior Mechanisms 0.010 1.000 1 2008 2008
dbSNP: rs1800044
rs1800044 		0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		Mental Disorders 0.010 1.000 1 2009 2009
dbSNP: rs1800044
rs1800044 		0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03
CUI: C0027849
Disease: Neuroleptic Malignant Syndrome
Neuroleptic Malignant Syndrome 		Nervous System Diseases; Chemically-Induced Disorders 0.010 1.000 1 1998 1998
dbSNP: rs1800044
rs1800044 		0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03
CUI: C0344315
Disease: Depressed mood
Depressed mood 		Behavior and Behavior Mechanisms 0.010 1.000 1 2009 2009
dbSNP: rs1800044
rs1800044 		0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03
CUI: C0004936
Disease: Mental disorders
Mental disorders 		Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs1800044
rs1800044 		0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03
CUI: C0040517
Disease: Gilles de la Tourette syndrome
Gilles de la Tourette syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Mental Disorders 0.010 1.000 1 1996 1996
dbSNP: rs1800044
rs1800044 		0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03
CUI: C0011570
Disease: Mental Depression
Mental Depression 		Behavior and Behavior Mechanisms 0.010 1.000 1 2009 2009
dbSNP: rs6295
rs6295 		0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0014544
Disease: Epilepsy
Epilepsy 		Nervous System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs6295
rs6295 		0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0005587
Disease: Depression, Bipolar
Depression, Bipolar 		Mental Disorders 0.010 1.000 1 2011 2011
dbSNP: rs6295
rs6295 		0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0009087
Disease: Cluster C personality disorder
Cluster C personality disorder 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs6295
rs6295 		0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0001818
Disease: Agoraphobia
Agoraphobia 		Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs6295
rs6295 		0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0030193
Disease: Pain
Pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2012 2012
dbSNP: rs6295
rs6295 		0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0338614
Disease: Psychotic episodes
Psychotic episodes 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs6295
rs6295 		0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0006012
Disease: Borderline Personality Disorder
Borderline Personality Disorder 		Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs6295
rs6295 		0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0025193
Disease: Melancholia
Melancholia 		Mental Disorders 0.010 1.000 1 2008 2008
dbSNP: rs6295
rs6295 		0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0009086
Disease: Cluster B personality disorder
Cluster B personality disorder 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs6295
rs6295 		0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		Nervous System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs6295
rs6295 		0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0031212
Disease: Personality Disorders
Personality Disorders 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs6295
rs6295 		0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0748061
Disease: psychiatric hospitalization
psychiatric hospitalization 		0.010 1.000 1 2016 2016
dbSNP: rs6295
rs6295 		0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0853193
Disease: Bipolar I disorder
Bipolar I disorder 		Mental Disorders 0.010 1.000 1 2014 2014