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
|
990 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.100 | 0.957 | 70 | 1998 | 2019 | ||||||
Familial (FPAH)
|
276 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.080 | 1.000 | 8 | 2000 | 2019 | ||||||
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
|
5 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.800 | 1.000 | 7 | 1997 | 2015 | ||||||
Central neuroblastoma
|
231 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.060 | 1.000 | 6 | 2003 | 2018 | ||||||
Childhood Neuroblastoma
|
231 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.060 | 1.000 | 6 | 2003 | 2018 | ||||||
Neuroblastoma
|
386 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.060 | 1.000 | 6 | 2003 | 2018 | ||||||
Young onset Parkinson disease
|
32 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.060 | 1.000 | 6 | 2001 | 2019 | ||||||
Lewy Body Disease
|
41 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.030 | 1.000 | 3 | 2000 | 2004 | ||||||
Parkinson Disease, Familial, Type 1
|
27 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.030 | 1.000 | 3 | 1999 | 2006 | ||||||
Impaired cognition
|
348 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.020 | 0.500 | 2 | 2001 | 2019 | ||||||
Neurodegenerative Disorders
|
85 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.020 | 1.000 | 2 | 2002 | 2003 | ||||||
Parkinsonian Disorders
|
95 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.020 | 1.000 | 2 | 2001 | 2019 | ||||||
Tremor
|
52 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.020 | 1.000 | 2 | 2003 | 2004 | ||||||
Brain Diseases
|
10 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
Cognition Disorders
|
47 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.010 | 1 | 2019 | 2019 | |||||||
Huntington Disease
|
115 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.010 | 1.000 | 1 | 2007 | 2007 | ||||||
Hyperactive behavior
|
112 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.010 | 1.000 | 1 | 2011 | 2011 | ||||||
Lewy Body Variant of Alzheimer Disease
|
2 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.010 | 1.000 | 1 | 2000 | 2000 | ||||||
Motor Disorders
|
2 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.010 | 1.000 | 1 | 2003 | 2003 | ||||||
Movement Disorders
|
247 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.010 | 1.000 | 1 | 2017 | 2017 | ||||||
Muscle Rigidity
|
25 | 0.732 | 0.160 | 4 | 89835580 | missense variant | C/G | snv | 0.010 | 1.000 | 1 | 2003 | 2003 |