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.
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
121 0.614 0.360 4 89828149 missense variant C/T snv 0.020 1.000 2 2010 2019
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
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.614 0.360 4 89828149 missense variant C/T snv 0.040 0.750 4 1998 2018
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
CUI: C2751492
Disease: 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
CUI: C4551993
Disease: Amyotrophic Lateral Sclerosis, Familial
68 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2008 2008
Anxiety
CUI: C0003467
Disease: Anxiety
287 0.614 0.360 4 89828149 missense variant C/T snv 0.030 1.000 3 2013 2020
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
163 0.614 0.360 4 89828149 missense variant C/T snv 0.030 1.000 3 2013 2020
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
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
231 0.614 0.360 4 89828149 missense variant C/T snv 0.050 1.000 5 2003 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
Childhood Neuroblastoma
CUI: C4086165
Disease: Childhood Neuroblastoma
231 0.614 0.360 4 89828149 missense variant C/T snv 0.050 1.000 5 2003 2018
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
Dementia
CUI: C0497327
Disease: Dementia
176 0.614 0.360 4 89828149 missense variant C/T snv 0.030 1.000 3 2017 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
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.614 0.360 4 89828149 missense variant C/T snv 0.100 1.000 13 2000 2018
Fibrillation
CUI: C0232197
Disease: Fibrillation
8 0.614 0.360 4 89828149 missense variant C/T snv 0.070 1.000 7 2001 2018
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
Gastrointestinal dysfunction
CUI: C0679407
Disease: Gastrointestinal dysfunction
6 0.614 0.360 4 89828149 missense variant C/T snv 0.020 1.000 2 2018 2019