rs6311, HTR2A

N. diseases: 41
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Alzheimer disease, familial, type 3
CUI: C1843013
Disease: Alzheimer disease, familial, type 3
124 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2019 2019
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2019 2019
Amnesia
CUI: C0002622
Disease: Amnesia
12 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2015 2015
Anxiety
CUI: C0003467
Disease: Anxiety
287 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2017 2017
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
163 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2017 2017
Attention deficit hyperactivity disorder
420 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2013 2013
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1 2016 2016
Borderline Personality Disorder
CUI: C0006012
Disease: Borderline Personality Disorder
82 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2014 2014
Cannabis Abuse
CUI: C0006868
Disease: Cannabis Abuse
8 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2012 2012
Cannabis use
CUI: C3160814
Disease: Cannabis use
44 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2012 2012
Chronic Fatigue Syndrome
CUI: C0015674
Disease: Chronic Fatigue Syndrome
14 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2011 2011
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2019 2019
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2017 2017
Drug abuse
CUI: C0013146
Disease: Drug abuse
39 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1 2014 2014
Drug habituation
CUI: C0013170
Disease: Drug habituation
19 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2018 2018
Eating Disorders
CUI: C0013473
Disease: Eating Disorders
42 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2019 2019
Female sexual dysfunction
CUI: C1112442
Disease: Female sexual dysfunction
3 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1 2014 2014
Fibromyalgia
CUI: C0016053
Disease: Fibromyalgia
38 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2008 2008
Gilles de la Tourette syndrome
CUI: C0040517
Disease: Gilles de la Tourette syndrome
63 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2007 2007
Impulsive character (finding)
CUI: C0564567
Disease: Impulsive character (finding)
19 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2006 2006
Memory Loss
CUI: C0751295
Disease: Memory Loss
10 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2015 2015
Mental Depression
CUI: C0011570
Disease: Mental Depression
271 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2017 2017
Mental disorders
CUI: C0004936
Disease: Mental disorders
149 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2017 2017
Pain
CUI: C0030193
Disease: Pain
196 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2019 2019
Pervasive Development Disorder
CUI: C0524528
Disease: Pervasive Development Disorder
49 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2014 2014