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. | ||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Alzheimer's Disease
|
1843 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.900 | 0.913 | 23 | 2009 | 2018 | |||||
Alzheimer Disease, Late Onset
|
243 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.100 | 1.000 | 12 | 2010 | 2018 | |||||
Mild cognitive disorder
|
96 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.040 | 1.000 | 4 | 2013 | 2019 | |||||
Impaired cognition
|
348 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.020 | 1.000 | 2 | 2013 | 2018 | |||||
AURAL ATRESIA, CONGENITAL
|
29 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||
Autoantibody measurement
|
52 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.700 | 1.000 | 1 | 2009 | 2009 | |||||
Cognition Disorders
|
47 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||
Dementia
|
176 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||
Diabetes
|
710 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||
Diabetes Mellitus
|
824 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.010 | 1.000 | 1 | 2019 | 2019 | |||||
Forgetful
|
18 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||
Gestational Diabetes
|
224 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||
Impaired glucose tolerance
|
81 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.010 | 1.000 | 1 | 2017 | 2017 | |||||
Memory impairment
|
48 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.010 | 1.000 | 1 | 2016 | 2016 | |||||
Mental deterioration
|
121 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.010 | 1.000 | 1 | 2013 | 2013 | |||||
Parkinson Disease
|
990 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.010 | 1.000 | 1 | 2011 | 2011 | |||||
Presenile dementia
|
159 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.010 | 1.000 | 1 | 2014 | 2014 | |||||
Prion Diseases
|
67 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.700 | 1.000 | 1 | 2012 | 2012 | |||||
Schizophrenia
|
2897 | 0.752 | 0.160 | 8 | 27607002 | intron variant | T/C | snv | 0.56 | 0.010 | 1.000 | 1 | 2010 | 2010 |