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.
Memory impairment
CUI: C0233794
Disease: Memory impairment
48 0.614 0.360 4 89828149 missense variant C/T snv 0.020 1.000 2 2013 2019
Sleep Disorders
CUI: C0851578
Disease: Sleep Disorders
38 0.614 0.360 4 89828149 missense variant C/T snv 0.020 1.000 2 2013 2015
Sleep disturbances
CUI: C0037317
Disease: Sleep disturbances
74 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2013 2013
[D]Sleep disturbances (& [hypersomnia] or [insomnia])
CUI: C0947785
Disease: [D]Sleep disturbances (& [hypersomnia] or [insomnia])
23 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2013 2013
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
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
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
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
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
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
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
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
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