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: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0334533
Disease: Arteriovenous hemangioma
Arteriovenous hemangioma
0.010 1.000 1 2012 2012
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0013170
Disease: Drug habituation
Drug habituation
0.010 1.000 1 2017 2017
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0220612
Disease: Childhood Non-Hodgkin Lymphoma
Childhood Non-Hodgkin Lymphoma
0.010 1.000 1 2019 2019
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0549622
Disease: Sexual Dysfunction
Sexual Dysfunction
0.010 1.000 1 2019 2019
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0699885
Disease: Carcinoma of bladder
Carcinoma of bladder
0.010 1.000 1 2018 2018
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C1535926
Disease: Neurodevelopmental Disorders
Neurodevelopmental Disorders
0.010 1.000 1 2020 2020
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.010 1.000 1 2007 2007
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0005956
Disease: Bone Marrow Diseases
Bone Marrow Diseases
0.010 1.000 1 2016 2016
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0009398
Disease: Color vision defect
Color vision defect
0.010 1.000 1 2011 2011
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.010 1.000 1 2009 2009
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C2700439
Disease: MAJOR AFFECTIVE DISORDER 8
MAJOR AFFECTIVE DISORDER 8
0.010 1.000 1 2004 2004
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0858853
Disease: Impulsive aggression
Impulsive aggression
0.010 1.000 1 2010 2010
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0038644
Disease: Sudden infant death syndrome
Sudden infant death syndrome
0.010 1.000 1 2011 2011
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0011253
Disease: Delusions
Delusions
0.010 1.000 1 2008 2008
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0031212
Disease: Personality Disorders
Personality Disorders
0.010 1.000 1 2009 2009
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions
0.010 1.000 1 2004 2004
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
Frontotemporal Lobar Degeneration
0.010 1.000 1 2012 2012
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0085271
Disease: Self-Injurious Behavior
Self-Injurious Behavior
0.010 1.000 1 2013 2013
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0221074
Disease: Depression, Postpartum
Depression, Postpartum
0.010 1.000 1 2010 2010
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C4237343
Disease: Overweight or obesity
Overweight or obesity
0.010 < 0.001 1 2013 2013
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0751039
Disease: Cockayne Syndrome, Type I
Cockayne Syndrome, Type I
0.010 1.000 1 2020 2020
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C1852197
Disease: MAJOR AFFECTIVE DISORDER 1
MAJOR AFFECTIVE DISORDER 1
0.010 1.000 1 2004 2004
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
Hamartoma Syndrome, Multiple
0.010 1.000 1 2017 2017
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C3805054
Disease: Prodromal Alzheimer's disease
Prodromal Alzheimer's disease
0.010 1.000 1 2014 2014
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
Multiple Sclerosis, Relapsing-Remitting
0.010 1.000 1 2009 2009