Gene: APOA1 ×
Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912724
rs121912724
APOA1 ; APOA1-AS
0.800 GeneticVariation UNIPROT Familial nephropathic systemic amyloidosis caused by apolipoprotein AI variant Arg26. 8208902

1994
dbSNP: rs121912724
rs121912724
APOA1 ; APOA1-AS
0.800 GeneticVariation UNIPROT Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis. 1502149

1992
dbSNP: rs121912724
rs121912724
APOA1 ; APOA1-AS
0.800 GeneticVariation UNIPROT A mutation in apolipoprotein A-I in the Iowa type of familial amyloidotic polyneuropathy. 2123470

1990
dbSNP: rs121912724
rs121912724
APOA1 ; APOA1-AS
0.800 GeneticVariation UNIPROT Variant apolipoprotein AI as a major constituent of a human hereditary amyloid. 3142462

1988
dbSNP: rs121912724
rs121912724
APOA1 ; APOA1-AS
C 0.800 CausalMutation CLINVAR

dbSNP: rs28931574
rs28931574
APOA1 ; APOA1-AS
0.700 GeneticVariation UNIPROT Familial nephropathic systemic amyloidosis caused by apolipoprotein AI variant Arg26. 8208902

1994
dbSNP: rs28931574
rs28931574
APOA1 ; APOA1-AS
0.700 GeneticVariation UNIPROT Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis. 1502149

1992
dbSNP: rs28931574
rs28931574
APOA1 ; APOA1-AS
0.700 GeneticVariation UNIPROT A mutation in apolipoprotein A-I in the Iowa type of familial amyloidotic polyneuropathy. 2123470

1990
dbSNP: rs28931574
rs28931574
APOA1 ; APOA1-AS
0.700 GeneticVariation UNIPROT Variant apolipoprotein AI as a major constituent of a human hereditary amyloid. 3142462

1988
dbSNP: rs121912726
rs121912726
APOA1 ; APOA1-AS
G 0.700 CausalMutation CLINVAR

dbSNP: rs121912729
rs121912729
APOA1 ; APOA1-AS
G 0.700 CausalMutation CLINVAR

dbSNP: rs121912730
rs121912730
APOA1 ; APOA1-AS
G 0.700 CausalMutation CLINVAR