rs104893877, SNCA

N. diseases: 59
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.
Adenomatous Polyposis Coli
CUI: C0032580
Disease: Adenomatous Polyposis Coli
237 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2010 2010
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2016 2016
Amyloid Neuropathies, Familial
CUI: C0206245
Disease: Amyloid Neuropathies, Familial
16 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2010 2010
AMYLOIDOSIS, HEREDITARY, TRANSTHYRETIN-RELATED
68 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2010 2010
Amyotrophic Lateral Sclerosis, Familial
68 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2008 2008
Autosomal Dominant Parkinsonism
CUI: C0752098
Disease: Autosomal Dominant Parkinsonism
3 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 1998 1998
Behavioral Symptoms
CUI: C0004941
Disease: Behavioral Symptoms
9 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2012 2012
Brain Diseases
CUI: C0006111
Disease: Brain Diseases
10 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2018 2018
Caffeine related disorders
CUI: C0236734
Disease: Caffeine related disorders
56 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1 2018 2018
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2016 2016
CNS metastases
CUI: C0686377
Disease: CNS metastases
14 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2019 2019
Cognition Disorders
CUI: C0009241
Disease: Cognition Disorders
47 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2018 2018
Dystonia
CUI: C0013421
Disease: Dystonia
97 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2015 2015
Forgetful
CUI: C0542476
Disease: Forgetful
18 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2019 2019
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1 2017 2017
Gaucher Disease
CUI: C0017205
Disease: Gaucher Disease
82 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2017 2017
Gaucher Disease, Type 1
CUI: C1961835
Disease: Gaucher Disease, Type 1
124 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2017 2017
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2016 2016
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2016 2016
Lewy Body Variant of Alzheimer Disease
2 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2000 2000
Mental disorders
CUI: C0004936
Disease: Mental disorders
149 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2019 2019
Mitochondrial abnormalities
CUI: C4020732
Disease: Mitochondrial abnormalities
20 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2007 2007
Multiple Chronic Conditions
CUI: C3266262
Disease: Multiple Chronic Conditions
42 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2016 2016
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1 2017 2017
Progressive cGVHD
CUI: C3539781
Disease: Progressive cGVHD
40 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2008 2008