rs63750579, APP

N. diseases: 13
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.
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
5 0.742 0.280 21 25891856 missense variant C/G;T snv 0.800 1.000 6 1990 2010
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.742 0.280 21 25891856 missense variant C/G;T snv 0.020 1.000 2 2000 2002
AURAL ATRESIA, CONGENITAL
CUI: C1842937
Disease: AURAL ATRESIA, CONGENITAL
29 0.742 0.280 21 25891856 missense variant C/G;T snv 0.020 1.000 2 2004 2018
Cerebral Amyloid Angiopathy
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
22 0.742 0.280 21 25891856 missense variant C/G;T snv 0.020 1.000 2 2004 2018
Cerebral Amyloid Angiopathy, Hereditary
4 0.742 0.280 21 25891856 missense variant C/G;T snv 0.020 1.000 2 2000 2010
Cerebral hemorrhage with amyloidosis, hereditary, Dutch type
2 0.742 0.280 21 25891856 missense variant C/G;T snv 0.020 1.000 2 2007 2018
Anxiety
CUI: C0003467
Disease: Anxiety
287 0.742 0.280 21 25891856 missense variant C/G;T snv 0.010 1.000 1 2015 2015
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
163 0.742 0.280 21 25891856 missense variant C/G;T snv 0.010 1.000 1 2015 2015
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.742 0.280 21 25891856 missense variant C/G;T snv 0.010 1.000 1 2002 2002
Dementia
CUI: C0497327
Disease: Dementia
176 0.742 0.280 21 25891856 missense variant C/G;T snv 0.010 1.000 1 2004 2004
Plaque, Amyloid
CUI: C2936349
Disease: Plaque, Amyloid
10 0.742 0.280 21 25891856 missense variant C/G;T snv 0.010 1.000 1 2010 2010
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.742 0.280 21 25891856 missense variant C/G;T snv 0.010 1.000 1 2004 2004
Senile Plaques
CUI: C0333463
Disease: Senile Plaques
21 0.742 0.280 21 25891856 missense variant C/G;T snv 0.010 1.000 1 2010 2010