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.
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
Rumination Disorders
CUI: C0154575
Disease: Rumination Disorders
13 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2019 2019
Sexual desire disorder
CUI: C0036904
Disease: Sexual desire disorder
1 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1 2013 2013
Sexual Dysfunction
CUI: C0549622
Disease: Sexual Dysfunction
12 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2013 2013
Suicidal
CUI: C0438696
Disease: Suicidal
29 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2006 2006
Wolfram Syndrome 1
CUI: C4551693
Disease: Wolfram Syndrome 1
36 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.010 1.000 1 2006 2006