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 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.100 | 0.980 | 153 | 1997 | 2020 | ||||||
Sporadic Parkinson disease
|
65 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.040 | 1.000 | 4 | 2001 | 2020 | ||||||
Anxiety
|
287 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.030 | 1.000 | 3 | 2013 | 2020 | ||||||
Anxiety Disorders
|
163 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.030 | 1.000 | 3 | 2013 | 2020 | ||||||
Motor symptoms
|
15 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.030 | 1.000 | 3 | 2018 | 2020 | ||||||
Parkinsonian Disorders
|
95 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.070 | 0.857 | 7 | 2001 | 2019 | ||||||
Abnormal behavior
|
121 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.020 | 1.000 | 2 | 2010 | 2019 | ||||||
Gastrointestinal dysfunction
|
6 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.020 | 1.000 | 2 | 2018 | 2019 | ||||||
Memory impairment
|
48 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.020 | 1.000 | 2 | 2013 | 2019 | ||||||
nervous system disorder
|
39 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.020 | 1.000 | 2 | 2019 | 2019 | ||||||
CNS metastases
|
14 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
Forgetful
|
18 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
Mental disorders
|
149 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
Familial (FPAH)
|
276 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.100 | 1.000 | 13 | 2000 | 2018 | ||||||
Fibrillation
|
8 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.070 | 1.000 | 7 | 2001 | 2018 | ||||||
Parkinson Disease, Familial, Type 1
|
27 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.070 | 1.000 | 7 | 1998 | 2018 | ||||||
Central neuroblastoma
|
231 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.050 | 1.000 | 5 | 2003 | 2018 | ||||||
Childhood Neuroblastoma
|
231 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.050 | 1.000 | 5 | 2003 | 2018 | ||||||
Neuroblastoma
|
386 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.050 | 1.000 | 5 | 2003 | 2018 | ||||||
Alzheimer's Disease
|
1843 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.040 | 0.750 | 4 | 1998 | 2018 | ||||||
Hyperactive behavior
|
112 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.040 | 1.000 | 4 | 2006 | 2018 | ||||||
Dementia
|
176 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.030 | 1.000 | 3 | 2017 | 2018 | ||||||
Impaired cognition
|
348 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.030 | 1.000 | 3 | 2013 | 2018 | ||||||
Presenile dementia
|
159 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.030 | 1.000 | 3 | 2017 | 2018 | ||||||
Brain Diseases
|
10 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2018 | 2018 |