Source: ALL

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: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0233488
Disease: Feeling despair
Feeling despair
0.010 1.000 1 2017 2017
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0011603
Disease: Dermatitis
Dermatitis
0.010 1.000 1 2017 2017
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0859021
Disease: Hyperthymic state
Hyperthymic state
0.010 1.000 1 2008 2008
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C3714756
Disease: Intellectual Disability
Intellectual Disability
0.010 1.000 1 2010 2010
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0154409
Disease: Recurrent major depressive episodes
Recurrent major depressive episodes
0.010 1.000 1 2011 2011
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0236969
Disease: Substance-Related Disorders
Substance-Related Disorders
0.010 1.000 1 2007 2007
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0520680
Disease: Sleep Apnea, Central
Sleep Apnea, Central
0.010 1.000 1 2020 2020
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C1279420
Disease: Anxiety neurosis (finding)
Anxiety neurosis (finding)
0.010 1.000 1 2017 2017
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0235946
Disease: Cerebral atrophy
Cerebral atrophy
0.010 1.000 1 2019 2019
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0086237
Disease: Epilepsy, Cryptogenic
Epilepsy, Cryptogenic
0.010 1.000 1 2016 2016
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0700613
Disease: Anxiety state
Anxiety state
0.010 1.000 1 2017 2017
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0001726
Disease: Affective Symptoms
Affective Symptoms
0.010 1.000 1 2016 2016
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0220605
Disease: Adult Non-Hodgkin Lymphoma
Adult Non-Hodgkin Lymphoma
0.010 1.000 1 2019 2019
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C2700438
Disease: MAJOR AFFECTIVE DISORDER 7
MAJOR AFFECTIVE DISORDER 7
0.010 1.000 1 2004 2004
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0036939
Disease: Shared Paranoid Disorder
Shared Paranoid Disorder
0.010 1.000 1 2015 2015
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 1.000 1 2009 2009
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0221074
Disease: Depression, Postpartum
Depression, Postpartum
0.010 1.000 1 2010 2010
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 1.000 1 2019 2019
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0085271
Disease: Self-Injurious Behavior
Self-Injurious Behavior
0.010 1.000 1 2013 2013
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0002622
Disease: Amnesia
Amnesia
0.010 < 0.001 1 2017 2017
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0522174
Disease: Delinquent behavior
Delinquent behavior
0.010 1.000 1 2014 2014
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0752347
Disease: Lewy Body Disease
Lewy Body Disease
0.010 < 0.001 1 2006 2006
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0334533
Disease: Arteriovenous hemangioma
Arteriovenous hemangioma
0.010 1.000 1 2012 2012
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.010 1.000 1 2009 2009
dbSNP: rs6265
rs6265
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
0.010 1.000 1 2016 2016