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.
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
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
Obsessive-Compulsive Disorder
CUI: C0028768
Disease: Obsessive-Compulsive Disorder
112 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.060 0.833 6 2007 2018
Impulsive Behavior
CUI: C0021125
Disease: Impulsive Behavior
69 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.020 1.000 2 2006 2018
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
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.100 0.800 10 2010 2019
Unipolar Depression
CUI: C0041696
Disease: Unipolar Depression
225 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.050 1.000 5 2010 2019
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.030 0.667 3 2014 2019
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
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
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
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
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
Psoriasis
CUI: C0033860
Disease: Psoriasis
705 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 0.020 1.000 2 2010 2020