Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0865424
Disease: Adult attention deficit hyperactivity disorder
Adult attention deficit hyperactivity disorder 		0.010 1.000 1 2010 2010
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0009087
Disease: Cluster C personality disorder
Cluster C personality disorder 		0.010 1.000 1 2010 2010
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0009241
Disease: Cognition Disorders
Cognition Disorders 		0.010 1.000 1 2014 2014
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0546983
Disease: Post-Concussion Syndrome
Post-Concussion Syndrome 		0.010 1.000 1 2014 2014
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0853193
Disease: Bipolar I disorder
Bipolar I disorder 		0.010 1.000 1 2014 2014
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0005587
Disease: Depression, Bipolar
Depression, Bipolar 		0.010 1.000 1 2011 2011
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0025193
Disease: Melancholia
Melancholia 		0.010 1.000 1 2008 2008
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0030193
Disease: Pain
Pain 		0.010 1.000 1 2012 2012
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0001818
Disease: Agoraphobia
Agoraphobia 		0.010 1.000 1 2017 2017
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0748061
Disease: psychiatric hospitalization
psychiatric hospitalization 		0.010 1.000 1 2016 2016
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 1.000 1 2014 2014
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0014556
Disease: Epilepsy, Temporal Lobe
Epilepsy, Temporal Lobe 		0.010 1.000 1 2013 2013
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0520676
Disease: Premenstrual Dysphoric Disorder
Premenstrual Dysphoric Disorder 		0.010 1.000 1 2014 2014
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0031212
Disease: Personality Disorders
Personality Disorders 		0.010 1.000 1 2010 2010
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0014544
Disease: Epilepsy
Epilepsy 		0.010 1.000 1 2013 2013
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0013170
Disease: Drug habituation
Drug habituation 		0.010 1.000 1 2018 2018
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0006012
Disease: Borderline Personality Disorder
Borderline Personality Disorder 		0.010 1.000 1 2008 2008
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C1864389
Disease: PREMATURE CHROMATID SEPARATION TRAIT
PREMATURE CHROMATID SEPARATION TRAIT 		0.010 1.000 1 2014 2014
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders 		0.010 1.000 1 2013 2013
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior 		0.010 1.000 1 2008 2008
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0036572
Disease: Seizures
Seizures 		0.010 1.000 1 2018 2018
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0009086
Disease: Cluster B personality disorder
Cluster B personality disorder 		0.010 1.000 1 2010 2010
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0338614
Disease: Psychotic episodes
Psychotic episodes 		0.010 1.000 1 2014 2014
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0852733
Disease: Completed Suicide
Completed Suicide 		0.010 1.000 1 2011 2011
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0438696
Disease: Suicidal
Suicidal 		0.010 1.000 1 2009 2009