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: 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: 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: 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: 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
dbSNP: rs6561334
rs6561334
13 46849989 intron variant G/A snv 6.4E-02
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement
0.700 1.000 1 2012 2012
dbSNP: rs6561334
rs6561334
13 46849989 intron variant G/A snv 6.4E-02
Low density lipoprotein cholesterol measurement
0.700 1.000 1 2012 2012
dbSNP: rs7330636
rs7330636
13 46849457 intron variant C/T snv 0.42
CUI: C0239377
Disease: Arm Pain
Arm Pain
Pathological Conditions, Signs and Symptoms 0.010 1.000 1 2019 2019
dbSNP: rs757096279
rs757096279
13 46835363 missense variant C/T snv 2.0E-05 7.0E-06
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
Cardiovascular Diseases 0.010 < 0.001 1 2013 2013
dbSNP: rs7984966
rs7984966
13 46855311 intron variant T/A;C snv
CUI: C0424101
Disease: Inattention
Inattention
0.010 1.000 1 2016 2016
dbSNP: rs9316235
rs9316235
13 46871568 intron variant G/A snv 0.19
CUI: C0525045
Disease: Mood Disorders
Mood Disorders
Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs9316235
rs9316235
13 46871568 intron variant G/A snv 0.19
CUI: C0013146
Disease: Drug abuse
Drug abuse
Chemically-Induced Disorders; Mental Disorders 0.010 1.000 1 2010 2010
dbSNP: rs6313
rs6313
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
Mental Disorders 0.100 0.810 42 1996 2019
dbSNP: rs6313
rs6313
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
Mental Disorders 0.100 0.933 15 2000 2019
dbSNP: rs6313
rs6313
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
Nervous System Diseases; Mental Disorders 0.100 0.917 12 2003 2019
dbSNP: rs6313
rs6313
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression
Mental Disorders 0.100 1.000 11 2000 2019
dbSNP: rs6313
rs6313
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40
CUI: C0438696
Disease: Suicidal
Suicidal
Behavior and Behavior Mechanisms 0.080 1.000 8 2000 2013
dbSNP: rs6313
rs6313
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40
CUI: C0033975
Disease: Psychotic Disorders
Psychotic Disorders
Mental Disorders 0.070 0.857 7 2007 2017
dbSNP: rs6313
rs6313
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40
CUI: C0030319
Disease: Panic Disorder
Panic Disorder
Mental Disorders 0.060 1.000 6 2001 2016
dbSNP: rs6313
rs6313
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40
CUI: C0349204
Disease: Nonorganic psychosis
Nonorganic psychosis
Mental Disorders 0.060 1.000 6 2007 2017
dbSNP: rs6313
rs6313
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40
CUI: C0021125
Disease: Impulsive Behavior
Impulsive Behavior
Behavior and Behavior Mechanisms 0.060 1.000 6 2002 2018
dbSNP: rs6313
rs6313
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
Mental Disorders 0.050 1.000 5 2006 2014
dbSNP: rs6313
rs6313
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder
Mental Disorders 0.050 1.000 5 2003 2014
dbSNP: rs6313
rs6313
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40
CUI: C0016053
Disease: Fibromyalgia
Fibromyalgia
Musculoskeletal Diseases; Nervous System Diseases 0.050 0.600 5 1999 2012