rs63750671, APP

N. diseases: 8
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.
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.790 0.240 21 25891858 missense variant G/C snv 0.760 1.000 26 1991 2016
Alzheimer disease type 1
CUI: C2931257
Disease: Alzheimer disease type 1
10 0.790 0.240 21 25891858 missense variant G/C snv 0.700 0
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
CUI: C2751536
Disease: CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
5 0.790 0.240 21 25891858 missense variant G/C snv 0.700 0
Amyloid angiopathy
CUI: C2931784
Disease: Amyloid angiopathy
3 0.790 0.240 21 25891858 missense variant G/C snv 0.010 1.000 1 1998 1998
Cerebral Amyloid Angiopathy
CUI: C0085220
Disease: Cerebral Amyloid Angiopathy
22 0.790 0.240 21 25891858 missense variant G/C snv 0.010 1.000 1 2002 2002
Cerebral Amyloid Angiopathy, Hereditary
CUI: C1510489
Disease: Cerebral Amyloid Angiopathy, Hereditary
4 0.790 0.240 21 25891858 missense variant G/C snv 0.010 1.000 1 2000 2000
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
591 0.790 0.240 21 25891858 missense variant G/C snv 0.010 1.000 1 2002 2002
Senile Plaques
CUI: C0333463
Disease: Senile Plaques
21 0.790 0.240 21 25891858 missense variant G/C snv 0.010 1.000 1 1998 1998