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: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
0.020 < 0.001 2 2014 2016
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0752203
Disease: Dystonia, Primary
Dystonia, Primary
0.020 < 0.001 2 2013 2014
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: 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: C1112442
Disease: Female sexual dysfunction
Female sexual dysfunction
0.010 < 0.001 1 2016 2016
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C4721453
Disease: Peripheral Nervous System Diseases
Peripheral Nervous System Diseases
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: 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: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis
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: C1504404
Disease: Hippocampal sclerosis
Hippocampal sclerosis
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: C0751295
Disease: Memory Loss
Memory Loss
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: C0014175
Disease: Endometriosis
Endometriosis
0.010 < 0.001 1 2012 2012
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0040761
Disease: Transposition of Great Vessels
Transposition of Great Vessels
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: 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: C0038525
Disease: Subarachnoid Hemorrhage
Subarachnoid Hemorrhage
0.020 0.500 2 2007 2008
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C1392786
Disease: Cognitive changes
Cognitive changes
0.020 0.500 2 2006 2019
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.020 0.500 2 2006 2013
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.020 0.500 2 2010 2013
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0149931
Disease: Migraine Disorders
Migraine Disorders
0.020 0.500 2 2008 2015
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0006287
Disease: Bronchopulmonary Dysplasia
Bronchopulmonary Dysplasia
0.070 0.571 7 2003 2015
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0002726
Disease: Amyloidosis
Amyloidosis
0.050 0.600 5 2013 2017
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C0006012
Disease: Borderline Personality Disorder
Borderline Personality Disorder
0.090 0.667 9 2003 2017
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C1842981
Disease: NEUROTICISM
NEUROTICISM
0.060 0.667 6 2005 2016
dbSNP: rs759834365
rs759834365
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05
CUI: C1270972
Disease: Mild cognitive disorder
Mild cognitive disorder
0.060 0.667 6 2008 2020