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
|
121 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.020 | 1.000 | 2 | 2010 | 2019 | ||||||
Adenomatous Polyposis Coli
|
237 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
Adult Glioblastoma
|
98 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||
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
|
16 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2010 | 2010 | ||||||
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
|
68 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2008 | 2008 | ||||||
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 | ||||||
Autosomal Dominant Parkinsonism
|
3 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 1998 | 1998 | ||||||
Behavioral Symptoms
|
9 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2012 | 2012 | ||||||
Brain Diseases
|
10 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
Caffeine related disorders
|
56 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1 | 2018 | 2018 | |||||||
Central neuroblastoma
|
231 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.050 | 1.000 | 5 | 2003 | 2018 | ||||||
Childhood Glioblastoma
|
98 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2016 | 2016 | ||||||
Childhood Neuroblastoma
|
231 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.050 | 1.000 | 5 | 2003 | 2018 | ||||||
CNS metastases
|
14 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
Cognition Disorders
|
47 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2018 | 2018 | ||||||
Dementia
|
176 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.030 | 1.000 | 3 | 2017 | 2018 | ||||||
Dystonia
|
97 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2015 | 2015 | ||||||
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 | ||||||
Forgetful
|
18 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1.000 | 1 | 2019 | 2019 | ||||||
Frontotemporal dementia
|
215 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.010 | 1 | 2017 | 2017 | |||||||
Gastrointestinal dysfunction
|
6 | 0.614 | 0.360 | 4 | 89828149 | missense variant | C/T | snv | 0.020 | 1.000 | 2 | 2018 | 2019 |