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: rs7997012
rs7997012 		0.807 0.080 13 46837850 intron variant A/G snv 0.69
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.030 1.000 3 2011 2019
dbSNP: rs7997012
rs7997012 		0.807 0.080 13 46837850 intron variant A/G snv 0.69
CUI: C0270549
Disease: Generalized Anxiety Disorder
Generalized Anxiety Disorder 		Mental Disorders 0.020 1.000 2 2013 2013
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: rs1475196
rs1475196 		1.000 0.040 13 46881488 intron variant A/C snv 1.4E-03
CUI: C0853193
Disease: Bipolar I disorder
Bipolar I disorder 		Mental Disorders 0.010 1.000 1 2014 2014
dbSNP: rs17069005
rs17069005 		1.000 0.080 13 46849983 intron variant A/G snv 0.11
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.010 1.000 1 2017 2017
dbSNP: rs1923884
rs1923884 		1.000 0.120 13 46847701 intron variant C/T snv 0.12
CUI: C0015674
Disease: Chronic Fatigue Syndrome
Chronic Fatigue Syndrome 		Infections; Musculoskeletal Diseases; Nervous System Diseases 0.010 1.000 1 2008 2008
dbSNP: rs1923884
rs1923884 		1.000 0.120 13 46847701 intron variant C/T snv 0.12
CUI: C0235162
Disease: Difficulty sleeping
Difficulty sleeping 		Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs1923885
rs1923885 		1.000 0.040 13 46848951 intron variant T/C snv 0.43
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		Mental Disorders 0.010 1.000 1 2017 2017
dbSNP: rs1923886
rs1923886 		13 46849156 intron variant C/T snv 0.64
CUI: C0239377
Disease: Arm Pain
Arm Pain 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2019 2019
dbSNP: rs1928040
rs1928040 		1.000 0.040 13 46873101 intron variant G/A snv 0.49
CUI: C0024517
Disease: Major depression, single episode
Major depression, single episode 		Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs2070040
rs2070040 		13 46893491 intron variant G/A snv 0.37
CUI: C0235162
Disease: Difficulty sleeping
Difficulty sleeping 		Mental Disorders 0.010 1.000 1 2016 2016
dbSNP: rs2296972
rs2296972 		0.925 0.080 13 46854336 intron variant A/C snv 0.70
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs2296972
rs2296972 		0.925 0.080 13 46854336 intron variant A/C snv 0.70
CUI: C0006370
Disease: Bulimia
Bulimia 		Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2014 2014
dbSNP: rs2296972
rs2296972 		0.925 0.080 13 46854336 intron variant A/C snv 0.70
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.010 1.000 1 2017 2017
dbSNP: rs2296972
rs2296972 		0.925 0.080 13 46854336 intron variant A/C snv 0.70
CUI: C0030319
Disease: Panic Disorder
Panic Disorder 		Mental Disorders 0.010 1.000 1 2007 2007
dbSNP: rs2770292
rs2770292 		1.000 0.040 13 46860971 intron variant C/G snv 0.18
CUI: C0030319
Disease: Panic Disorder
Panic Disorder 		Mental Disorders 0.010 1.000 1 2007 2007
dbSNP: rs3742278
rs3742278 		1.000 0.040 13 46845442 intron variant A/G snv 0.19
CUI: C0030319
Disease: Panic Disorder
Panic Disorder 		Mental Disorders 0.010 1.000 1 2007 2007
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: rs643627
rs643627 		1.000 0.040 13 46854476 intron variant T/C snv 0.27
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		Mental Disorders 0.010 1.000 1 2018 2018
dbSNP: rs6561333
rs6561333 		1.000 0.080 13 46846177 intron variant T/C snv 0.60
CUI: C0600427
Disease: Cocaine Dependence
Cocaine Dependence 		Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2013 2013
dbSNP: rs6561334
rs6561334 		13 46849989 intron variant G/A snv 6.4E-02
CUI: C1445957
Disease: Serum total cholesterol measurement
Serum total cholesterol measurement 		0.700 1.000 1 2012 2012
dbSNP: rs6561334
rs6561334 		13 46849989 intron variant G/A snv 6.4E-02
CUI: C0428474
Disease: Serum LDL cholesterol measurement
Serum LDL cholesterol measurement 		0.700 1.000 1 2012 2012