APP, amyloid beta precursor protein, 351

N. diseases: 485; N. variants: 114
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63749810
rs63749810
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2751536
Disease:
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
0.800 GeneticVariation UNIPROT
dbSNP: rs63749810
rs63749810
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2751536
Disease:
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
T 0.800 CausalMutation CLINVAR
dbSNP: rs63750579
rs63750579
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2751536
Disease:
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
T 0.800 CausalMutation CLINVAR
dbSNP: rs63750579
rs63750579
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2751536
Disease:
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
G 0.800 CausalMutation CLINVAR
dbSNP: rs63751039
rs63751039
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C0002395
Disease:
Alzheimer's Disease
0.790 GeneticVariation UNIPROT
dbSNP: rs193922916
rs193922916
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C0002395
Disease:
Alzheimer's Disease
A 0.740 CausalMutation CLINVAR
dbSNP: rs63750973
rs63750973
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C0002395
Disease:
Alzheimer's Disease
0.720 GeneticVariation UNIPROT
dbSNP: rs63751122
rs63751122
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C0002395
Disease:
Alzheimer's Disease
0.710 GeneticVariation UNIPROT
dbSNP: rs281865161
rs281865161
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2931257
Disease:
Alzheimer disease type 1
GA 0.700 CausalMutation CLINVAR
dbSNP: rs63749964
rs63749964
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2931257
Disease:
Alzheimer disease type 1
C 0.700 CausalMutation CLINVAR
dbSNP: rs63750066
rs63750066
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2931257
Disease:
Alzheimer disease type 1
T 0.700 CausalMutation CLINVAR
dbSNP: rs63750264
rs63750264
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2931257
Disease:
Alzheimer disease type 1
A 0.700 CausalMutation CLINVAR
dbSNP: rs63750264
rs63750264
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2931257
Disease:
Alzheimer disease type 1
T 0.700 CausalMutation CLINVAR
dbSNP: rs63750264
rs63750264
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2931257
Disease:
Alzheimer disease type 1
G 0.700 CausalMutation CLINVAR
dbSNP: rs63750399
rs63750399
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2931257
Disease:
Alzheimer disease type 1
C 0.700 CausalMutation CLINVAR
dbSNP: rs63750643
rs63750643
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2931257
Disease:
Alzheimer disease type 1
C 0.700 CausalMutation CLINVAR
dbSNP: rs63750671
rs63750671
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2751536
Disease:
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
C 0.700 CausalMutation CLINVAR
dbSNP: rs63750671
rs63750671
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2931257
Disease:
Alzheimer disease type 1
C 0.700 CausalMutation CLINVAR
dbSNP: rs63750734
rs63750734
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2931257
Disease:
Alzheimer disease type 1
T 0.700 CausalMutation CLINVAR
dbSNP: rs63750921
rs63750921
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2751536
Disease:
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
0.700 GeneticVariation UNIPROT
dbSNP: rs63750921
rs63750921
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C4015785
Disease:
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED, PIEDMONT VARIANT
C 0.700 CausalMutation CLINVAR
dbSNP: rs63750973
rs63750973
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2931257
Disease:
Alzheimer disease type 1
A 0.700 CausalMutation CLINVAR
dbSNP: rs63751039
rs63751039
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2751536
Disease:
CEREBRAL AMYLOID ANGIOPATHY, APP-RELATED
C 0.700 CausalMutation CLINVAR
dbSNP: rs63751039
rs63751039
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C2931257
Disease:
Alzheimer disease type 1
C 0.700 CausalMutation CLINVAR
dbSNP: rs63750264
rs63750264
Entrez Id: 351
Gene Symbol: APP
APP
CUI: C0002395
Disease:
Alzheimer's Disease
0.900 GeneticVariation UNIPROT A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid. 1302033 1992