Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs63749824
rs63749824
T 0.700 CausalMutation CLINVAR

dbSNP: rs63749836
rs63749836
A 0.700 GeneticVariation CLINVAR

dbSNP: rs63750308
rs63750308
G 0.700 CausalMutation CLINVAR

dbSNP: rs63750590
rs63750590
G 0.700 CausalMutation CLINVAR

dbSNP: rs63750635
rs63750635
T 0.700 CausalMutation CLINVAR

dbSNP: rs63750912
rs63750912
C 0.700 CausalMutation CLINVAR

dbSNP: rs63750972
rs63750972
T 0.700 CausalMutation CLINVAR

dbSNP: rs63751035
rs63751035
GRN
C 0.700 CausalMutation CLINVAR

dbSNP: rs63751035
rs63751035
GRN
CTG 0.700 CausalMutation CLINVAR

dbSNP: rs63751223
rs63751223
C 0.700 GeneticVariation CLINVAR

dbSNP: rs63751394
rs63751394
C 0.700 CausalMutation CLINVAR

dbSNP: rs794729669
rs794729669
GRN
C 0.700 CausalMutation CLINVAR

dbSNP: rs794729670
rs794729670
GRN
G 0.700 CausalMutation CLINVAR

dbSNP: rs794729671
rs794729671
GRN
GT 0.700 CausalMutation CLINVAR

dbSNP: rs794729672
rs794729672
GRN
GC 0.700 CausalMutation CLINVAR

dbSNP: rs63750231
rs63750231
C 0.700 CausalMutation CLINVAR The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families. 7550356

1995

dbSNP: rs63750526
rs63750526
A 0.700 CausalMutation CLINVAR Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. 7596406

1995

dbSNP: rs661
rs661
A 0.700 CausalMutation CLINVAR Mutations of the presenilin I gene in families with early-onset Alzheimer's disease. 8634712

1995

dbSNP: rs661
rs661
A 0.700 CausalMutation CLINVAR Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. 7596406

1995

dbSNP: rs63750900
rs63750900
A 0.700 CausalMutation CLINVAR A further presenilin 1 mutation in the exon 8 cluster in familial Alzheimer's disease. 8910898

1996

dbSNP: rs63750526
rs63750526
A 0.700 CausalMutation CLINVAR Human presenilin-1, but not familial Alzheimer's disease (FAD) mutants, facilitate Caenorhabditis elegans Notch signalling independently of proteolytic processing. 9680315

1997

dbSNP: rs63750900
rs63750900
A 0.700 CausalMutation CLINVAR A novel presenilin-1 mutation: increased beta-amyloid and neurofibrillary changes. 9189043

1997

dbSNP: rs63751278
rs63751278
G 0.700 CausalMutation CLINVAR Early-onset Alzheimer's disease with a presenilin-1 mutation at the site corresponding to the Volga German presenilin-2 mutation. 9225696

1997

dbSNP: rs661
rs661
A 0.700 CausalMutation CLINVAR Human presenilin-1, but not familial Alzheimer's disease (FAD) mutants, facilitate Caenorhabditis elegans Notch signalling independently of proteolytic processing. 9680315

1997

dbSNP: rs661
rs661
A 0.700 CausalMutation CLINVAR Alzheimer's disease-associated presenilins 1 and 2: accelerated amyloid fibril formation of mutant 410 Cys-->Tyr and 141 Asn-->Ile peptides. 9196071

1997