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: C0011581
Disease: Depressive disorder
Depressive disorder 		0.070 1.000 7 2008 2019
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0344315
Disease: Depressed mood
Depressed mood 		0.070 1.000 7 2008 2019
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0011570
Disease: Mental Depression
Mental Depression 		0.070 1.000 7 2008 2019
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.060 1.000 6 2009 2017
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.050 1.000 5 2010 2020
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression 		0.050 1.000 5 2009 2017
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0003467
Disease: Anxiety
Anxiety 		0.040 1.000 4 2010 2018
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		0.030 1.000 3 2010 2018
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.030 1.000 3 2013 2019
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0004936
Disease: Mental disorders
Mental disorders 		0.030 1.000 3 2008 2016
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		0.030 1.000 3 2013 2015
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0024517
Disease: Major depression, single episode
Major depression, single episode 		0.020 1.000 2 2008 2011
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0030319
Disease: Panic Disorder
Panic Disorder 		0.020 0.500 2 2013 2017
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		0.020 1.000 2 2011 2013
dbSNP: rs6295
rs6295
HTR1A
0.645 0.200 5 63962738 intron variant C/G snv 0.49
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
Post-Traumatic Stress Disorder 		0.020 1.000 2 2016 2019
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: 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: C1864389
Disease: PREMATURE CHROMATID SEPARATION TRAIT
PREMATURE CHROMATID SEPARATION TRAIT 		0.010 1.000 1 2014 2014