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: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0748061
Disease: psychiatric hospitalization
psychiatric hospitalization
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: C0028756
Disease: Obesity, Morbid
Obesity, Morbid
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: C3536593
Disease: Chronic cerebrovascular accident
Chronic cerebrovascular accident
0.010 1.000 1 2014 2014
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0233488
Disease: Feeling despair
Feeling despair
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: C2700440
Disease: MAJOR AFFECTIVE DISORDER 9
MAJOR AFFECTIVE DISORDER 9
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: C1510472
Disease: Drug Dependence
Drug Dependence
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: 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: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
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: 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
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy
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: C0730557
Disease: Emotional abuse
Emotional abuse
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: C0021125
Disease: Impulsive Behavior
Impulsive Behavior
0.010 1.000 1 2014 2014
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: C0013595
Disease: Eczema
Eczema
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: C0349489
Disease: Fetal Hypoxia
Fetal Hypoxia
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: C0031117
Disease: Peripheral Neuropathy
Peripheral Neuropathy
0.010 < 0.001 1 2018 2018
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0002622
Disease: Amnesia
Amnesia
0.010 < 0.001 1 2017 2017
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0752347
Disease: Lewy Body Disease
Lewy Body Disease
0.010 < 0.001 1 2006 2006
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0242510
Disease: Drug usage
Drug usage
0.010 1.000 1 2015 2015
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C1862389
Disease: ATRIAL SEPTAL DEFECT 1
ATRIAL SEPTAL DEFECT 1
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: 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: C0015923
Disease: Fetal Alcohol Syndrome
Fetal Alcohol Syndrome
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: C0016053
Disease: Fibromyalgia
Fibromyalgia
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: C0338591
Disease: Amnesia, Transient Global
Amnesia, Transient Global
0.010 < 0.001 1 2008 2008
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0263361
Disease: Psoriasis vulgaris
Psoriasis vulgaris
0.010 1.000 1 2014 2014