rs63750264, APP

N. diseases: 17
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 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.900 1.000 58 1991 2019
Alzheimer disease type 1
CUI: C2931257
Disease: Alzheimer disease type 1
10 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.700 0
Familial Alzheimer Disease (FAD)
CUI: C0276496
Disease: Familial Alzheimer Disease (FAD)
95 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.100 0.909 11 1991 2019
Alzheimer Disease, Early Onset
CUI: C0750901
Disease: Alzheimer Disease, Early Onset
96 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.080 1.000 8 1996 2019
Abnormal behavior
CUI: C0233514
Disease: Abnormal behavior
121 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.020 1.000 2 2000 2010
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.020 1.000 2 1993 2005
Memory impairment
CUI: C0233794
Disease: Memory impairment
48 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.020 1.000 2 2000 2004
Senile Plaques
CUI: C0333463
Disease: Senile Plaques
21 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.020 1.000 2 1997 2000
Alzheimer disease, familial, type 3
CUI: C1843013
Disease: Alzheimer disease, familial, type 3
124 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.010 1.000 1 2019 2019
Anxiety
CUI: C0003467
Disease: Anxiety
287 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.010 1.000 1 2004 2004
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
163 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.010 1.000 1 2004 2004
Burkitt Lymphoma
CUI: C0006413
Disease: Burkitt Lymphoma
13 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.010 1.000 1 2004 2004
Complete Trisomy 21 Syndrome
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
77 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007
Dementia
CUI: C0497327
Disease: Dementia
176 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.010 1.000 1 2000 2000
Down Syndrome
CUI: C0013080
Disease: Down Syndrome
80 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.010 1.000 1 2007 2007
Familial Alzheimer's disease of early onset
33 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.010 1.000 1 2017 2017
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.716 0.360 21 25891784 missense variant C/A;G;T snv 0.010 1.000 1 2000 2000