Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs429358
rs429358
APOE
C 0.890 GeneticVariation CLINVAR

dbSNP: rs1799945
rs1799945
HFE ; LOC108783645
G 0.800 CausalMutation CLINVAR

dbSNP: rs63751039
rs63751039
APP
0.790 GeneticVariation UNIPROT

dbSNP: rs193922916
rs193922916
APP
A 0.740 CausalMutation CLINVAR

dbSNP: rs63750973
rs63750973
APP
0.720 GeneticVariation UNIPROT

dbSNP: rs63751122
rs63751122
APP
0.710 GeneticVariation UNIPROT

dbSNP: rs1561901881
rs1561901881
CSF1R
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1561905293
rs1561905293
CSF1R
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1566630910
rs1566630910
PSEN1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1566638673
rs1566638673
PSEN1
CTTA 0.700 GeneticVariation CLINVAR

dbSNP: rs1566656702
rs1566656702
PSEN1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1566657804
rs1566657804
PSEN1
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1567885728
rs1567885728
GRN
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1568339995
rs1568339995
MAPT
T 0.700 GeneticVariation CLINVAR

dbSNP: rs377498269
rs377498269
SORL1
0.700 GeneticVariation UNIPROT

dbSNP: rs63750009
rs63750009
PSEN1
C 0.700 GeneticVariation CLINVAR

dbSNP: rs63750219
rs63750219
PSEN1
A 0.700 GeneticVariation CLINVAR

dbSNP: rs747306346
rs747306346
SORL1
0.700 GeneticVariation UNIPROT

dbSNP: rs866101707
rs866101707
VCP
A 0.700 GeneticVariation CLINVAR

dbSNP: rs63750264
rs63750264
APP
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
dbSNP: rs63750671
rs63750671
APP
0.760 GeneticVariation UNIPROT A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid. 1302033

1992
dbSNP: rs63750066
rs63750066
APP
0.730 GeneticVariation UNIPROT A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid. 1302033

1992
dbSNP: rs63750734
rs63750734
APP
0.730 GeneticVariation UNIPROT A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid. 1302033

1992
dbSNP: rs63750064
rs63750064
APP
0.720 GeneticVariation UNIPROT A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid. 1302033

1992
dbSNP: rs63749964
rs63749964
APP
0.710 GeneticVariation UNIPROT A pathogenic mutation for probable Alzheimer's disease in the APP gene at the N-terminus of beta-amyloid. 1302033

1992