rs6295, HTR1A

N. diseases: 40
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.
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
121 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2008 2008
Adult attention deficit hyperactivity disorder
6 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2010 2010
Agoraphobia
CUI: C0001818
Disease: Agoraphobia
11 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2017 2017
Bipolar I disorder
CUI: C0853193
Disease: Bipolar I disorder
46 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2014 2014
Borderline Personality Disorder
CUI: C0006012
Disease: Borderline Personality Disorder
82 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2008 2008
Cluster B personality disorder
CUI: C0009086
Disease: Cluster B personality disorder
2 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2010 2010
Cluster C personality disorder
CUI: C0009087
Disease: Cluster C personality disorder
1 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2010 2010
Cognition Disorders
CUI: C0009241
Disease: Cognition Disorders
47 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2014 2014
Completed Suicide
CUI: C0852733
Disease: Completed Suicide
33 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2011 2011
Depression, Bipolar
CUI: C0005587
Disease: Depression, Bipolar
2 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2011 2011
Drug habituation
CUI: C0013170
Disease: Drug habituation
19 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2018 2018
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2013 2013
Epilepsy, Temporal Lobe
CUI: C0014556
Disease: Epilepsy, Temporal Lobe
33 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2013 2013
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2014 2014
Melancholia
CUI: C0025193
Disease: Melancholia
8 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2008 2008
Migraine Disorders
CUI: C0149931
Disease: Migraine Disorders
264 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2013 2013
Pain
CUI: C0030193
Disease: Pain
196 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2012 2012
Personality Disorders
CUI: C0031212
Disease: Personality Disorders
8 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2010 2010
Post-Concussion Syndrome
CUI: C0546983
Disease: Post-Concussion Syndrome
1 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2014 2014
PREMATURE CHROMATID SEPARATION TRAIT
10 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2014 2014
Premenstrual Dysphoric Disorder
CUI: C0520676
Disease: Premenstrual Dysphoric Disorder
4 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2014 2014
psychiatric hospitalization
CUI: C0748061
Disease: psychiatric hospitalization
4 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2016 2016
Psychotic episodes
CUI: C0338614
Disease: Psychotic episodes
6 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2014 2014
Seizures
CUI: C0036572
Disease: Seizures
553 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2018 2018
Suicidal
CUI: C0438696
Disease: Suicidal
29 0.645 0.200 5 63962738 intron variant C/G snv 0.49 0.010 1.000 1 2009 2009