HTR2A, 5-hydroxytryptamine receptor 2A, 3356

N. diseases: 289; N. variants: 34
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: rs75634836
rs75634836
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06
CUI: C0030319
Disease: Panic Disorder
Panic Disorder
Mental Disorders 0.020 1.000 2 2008 2012
dbSNP: rs12584920
rs12584920
1.000 0.040 13 46890902 intron variant G/C;T snv
CUI: C3178789
Disease: Widespread Chronic Pain
Widespread Chronic Pain
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2011 2011
dbSNP: rs1328674
rs1328674
1.000 0.120 13 46867572 intron variant T/C;G snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.010 1.000 1 2013 2013
dbSNP: rs1805055
rs1805055
0.882 0.120 13 46895833 missense variant G/C;T snv 2.0E-05; 1.8E-02
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 1997 1997
dbSNP: rs1805055
rs1805055
0.882 0.120 13 46895833 missense variant G/C;T snv 2.0E-05; 1.8E-02
CUI: C4694057
Disease: Taq1A POLYMORPHISM
Taq1A POLYMORPHISM
0.010 1.000 1 2007 2007
dbSNP: rs1805055
rs1805055
0.882 0.120 13 46895833 missense variant G/C;T snv 2.0E-05; 1.8E-02
CUI: C0027849
Disease: Neuroleptic Malignant Syndrome
Neuroleptic Malignant Syndrome
Nervous System Diseases; Chemically-Induced Disorders 0.010 1.000 1 1998 1998
dbSNP: rs1885884
rs1885884
13 46856141 non coding transcript exon variant C/A;G;T snv
CUI: C0013146
Disease: Drug abuse
Drug abuse
Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs1885884
rs1885884
13 46856141 non coding transcript exon variant C/A;G;T snv
CUI: C0525045
Disease: Mood Disorders
Mood Disorders
Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs3125
rs3125
0.925 0.080 13 46834716 3 prime UTR variant C/G;T snv
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs3125
rs3125
0.925 0.080 13 46834716 3 prime UTR variant C/G;T snv
CUI: C0011570
Disease: Mental Depression
Mental Depression
Behavior and Behavior Mechanisms 0.010 1.000 1 2019 2019
dbSNP: rs3125
rs3125
0.925 0.080 13 46834716 3 prime UTR variant C/G;T snv
CUI: C0344315
Disease: Depressed mood
Depressed mood
Behavior and Behavior Mechanisms 0.010 1.000 1 2019 2019
dbSNP: rs3125
rs3125
0.925 0.080 13 46834716 3 prime UTR variant C/G;T snv
CUI: C0154575
Disease: Rumination Disorders
Rumination Disorders
Mental Disorders 0.010 1.000 1 2019 2019
dbSNP: rs594242
rs594242
1.000 0.040 13 46883917 intron variant C/A;G snv
CUI: C0438696
Disease: Suicidal
Suicidal
Behavior and Behavior Mechanisms 0.010 1.000 1 2006 2006
dbSNP: rs594242
rs594242
1.000 0.040 13 46883917 intron variant C/A;G snv
CUI: C0564567
Disease: Impulsive character (finding)
Impulsive character (finding)
0.010 1.000 1 2006 2006
dbSNP: rs594242
rs594242
1.000 0.040 13 46883917 intron variant C/A;G snv
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior
Behavior and Behavior Mechanisms 0.010 1.000 1 2006 2006
dbSNP: rs75634836
rs75634836
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06
CUI: C0016053
Disease: Fibromyalgia
Fibromyalgia
Musculoskeletal Diseases; Nervous System Diseases 0.010 < 0.001 1 2012 2012
dbSNP: rs75634836
rs75634836
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06
CUI: C0424295
Disease: Hyperactive behavior
Hyperactive behavior
Pathological Conditions, Signs and Symptoms; Nervous System Diseases 0.010 1.000 1 2006 2006
dbSNP: rs75634836
rs75634836
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.010 1.000 1 2005 2005
dbSNP: rs75634836
rs75634836
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior
Behavior and Behavior Mechanisms 0.010 1.000 1 2006 2006
dbSNP: rs75634836
rs75634836
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs75634836
rs75634836
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06
CUI: C0011570
Disease: Mental Depression
Mental Depression
Behavior and Behavior Mechanisms 0.010 1.000 1 2013 2013
dbSNP: rs75634836
rs75634836
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs75634836
rs75634836
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06
CUI: C0344315
Disease: Depressed mood
Depressed mood
Behavior and Behavior Mechanisms 0.010 1.000 1 2013 2013
dbSNP: rs75634836
rs75634836
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06
CUI: C0424101
Disease: Inattention
Inattention
0.010 1.000 1 2006 2006
dbSNP: rs75634836
rs75634836
0.807 0.160 13 46835532 missense variant C/A;T snv 4.0E-06
CUI: C0564567
Disease: Impulsive character (finding)
Impulsive character (finding)
0.010 1.000 1 2010 2010