rs6265, BDNF;BDNF-AS

N. diseases: 272
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.
Atrial Septal Defects
CUI: C0018817
Disease: Atrial Septal Defects
96 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2016 2016
Autistic Disorder
CUI: C0004352
Disease: Autistic Disorder
395 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2019 2019
Bipolar I disorder
CUI: C0853193
Disease: Bipolar I disorder
46 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2005 2005
Bone Marrow Diseases
CUI: C0005956
Disease: Bone Marrow Diseases
3 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2016 2016
Brain atrophy
CUI: C4551584
Disease: Brain atrophy
46 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2019 2019
Brain Ischemia
CUI: C0007786
Disease: Brain Ischemia
5 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2014 2014
Bullous pemphigoid
CUI: C0030805
Disease: Bullous pemphigoid
11 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2018 2018
Cerebral atrophy
CUI: C0235946
Disease: Cerebral atrophy
44 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2019 2019
Childhood asthma
CUI: C0264408
Disease: Childhood asthma
317 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2015 2015
Childhood Non-Hodgkin Lymphoma
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
39 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2019 2019
Chronic cerebrovascular accident
CUI: C3536593
Disease: Chronic cerebrovascular accident
2 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2014 2014
Chronic pain
CUI: C0150055
Disease: Chronic pain
19 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2010 2010
CNS disorder
CUI: C0007682
Disease: CNS disorder
11 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2015 2015
Cockayne Syndrome, Type I
CUI: C0751039
Disease: Cockayne Syndrome, Type I
42 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2020 2020
Color vision defect
CUI: C0009398
Disease: Color vision defect
4 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2011 2011
Common Migraine
CUI: C0338480
Disease: Common Migraine
62 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2017 2017
Compulsive hoarding
CUI: C0424290
Disease: Compulsive hoarding
4 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2011 2011
Conduct Disorder
CUI: C0149654
Disease: Conduct Disorder
18 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2020 2020
Congenital arteriovenous malformation
23 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2012 2012
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2018 2018
Delinquent behavior
CUI: C0522174
Disease: Delinquent behavior
2 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2014 2014
Delusions
CUI: C0011253
Disease: Delusions
15 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2008 2008
Depression and Suicide
CUI: C1524032
Disease: Depression and Suicide
2 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2018 2018
Depression, Postpartum
CUI: C0221074
Disease: Depression, Postpartum
6 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2010 2010
Dermatitis
CUI: C0011603
Disease: Dermatitis
16 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2017 2017