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.
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.614 0.360 4 89828149 missense variant C/T snv 0.100 0.980 153 1997 2020
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
5 0.614 0.360 4 89828149 missense variant C/T snv 0.800 1.000 7 1997 2015
Young onset Parkinson disease
CUI: C4275179
Disease: Young onset Parkinson disease
32 0.614 0.360 4 89828149 missense variant C/T snv 0.040 0.750 4 1997 2002
Parkinson Disease, Familial, Type 1
CUI: C3489791
Disease: Parkinson Disease, Familial, Type 1
27 0.614 0.360 4 89828149 missense variant C/T snv 0.070 1.000 7 1998 2018
Lewy Body Disease
CUI: C0752347
Disease: Lewy Body Disease
41 0.614 0.360 4 89828149 missense variant C/T snv 0.760 1.000 6 1998 2010
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
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
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
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
Fibrillation
CUI: C0232197
Disease: Fibrillation
8 0.614 0.360 4 89828149 missense variant C/T snv 0.070 1.000 7 2001 2018
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.614 0.360 4 89828149 missense variant C/T snv 0.070 0.857 7 2001 2019
Sporadic Parkinson disease
CUI: C4511452
Disease: Sporadic Parkinson disease
65 0.614 0.360 4 89828149 missense variant C/T snv 0.040 1.000 4 2001 2020
Movement Disorders
CUI: C0026650
Disease: Movement Disorders
247 0.614 0.360 4 89828149 missense variant C/T snv 0.030 1.000 3 2002 2006
Neurodegenerative Disorders
CUI: C0524851
Disease: Neurodegenerative Disorders
85 0.614 0.360 4 89828149 missense variant C/T snv 0.020 1.000 2 2002 2003
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 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
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
386 0.614 0.360 4 89828149 missense variant C/T snv 0.050 1.000 5 2003 2018
PARKINSON DISEASE, LATE-ONSET
CUI: C3160718
Disease: PARKINSON DISEASE, LATE-ONSET
76 0.614 0.360 4 89828149 missense variant C/T snv 0.020 1.000 2 2003 2017
Hyperactive behavior
CUI: C0424295
Disease: Hyperactive behavior
112 0.614 0.360 4 89828149 missense variant C/T snv 0.040 1.000 4 2006 2018
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
115 0.614 0.360 4 89828149 missense variant C/T snv 0.030 1.000 3 2007 2013
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
Amyotrophic Lateral Sclerosis, Familial
68 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2008 2008
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
Progressive Neoplastic Disease
CUI: C0677932
Disease: Progressive Neoplastic Disease
40 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2008 2008
Secondary Parkinson Disease
CUI: C0030569
Disease: Secondary Parkinson Disease
1 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2008 2008