APOA1, apolipoprotein A1, 335

N. diseases: 416; N. variants: 32
Disease: Amyloidosis, familial visceral ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912724
rs121912724
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0268389
Disease:
Amyloidosis, familial visceral 		0.800 GeneticVariation UNIPROT Familial nephropathic systemic amyloidosis caused by apolipoprotein AI variant Arg26. 8208902 1994
dbSNP: rs121912724
rs121912724
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0268389
Disease:
Amyloidosis, familial visceral 		0.800 GeneticVariation UNIPROT Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis. 1502149 1992
dbSNP: rs121912724
rs121912724
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0268389
Disease:
Amyloidosis, familial visceral 		0.800 GeneticVariation UNIPROT A mutation in apolipoprotein A-I in the Iowa type of familial amyloidotic polyneuropathy. 2123470 1990
dbSNP: rs121912724
rs121912724
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0268389
Disease:
Amyloidosis, familial visceral 		0.800 GeneticVariation UNIPROT Variant apolipoprotein AI as a major constituent of a human hereditary amyloid. 3142462 1988
dbSNP: rs121912724
rs121912724
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0268389
Disease:
Amyloidosis, familial visceral 		C 0.800 CausalMutation CLINVAR
dbSNP: rs28931574
rs28931574
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0268389
Disease:
Amyloidosis, familial visceral 		0.700 GeneticVariation UNIPROT Familial nephropathic systemic amyloidosis caused by apolipoprotein AI variant Arg26. 8208902 1994
dbSNP: rs28931574
rs28931574
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0268389
Disease:
Amyloidosis, familial visceral 		0.700 GeneticVariation UNIPROT Apolipoprotein AI mutation Arg-60 causes autosomal dominant amyloidosis. 1502149 1992
dbSNP: rs28931574
rs28931574
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0268389
Disease:
Amyloidosis, familial visceral 		0.700 GeneticVariation UNIPROT A mutation in apolipoprotein A-I in the Iowa type of familial amyloidotic polyneuropathy. 2123470 1990
dbSNP: rs28931574
rs28931574
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0268389
Disease:
Amyloidosis, familial visceral 		0.700 GeneticVariation UNIPROT Variant apolipoprotein AI as a major constituent of a human hereditary amyloid. 3142462 1988
dbSNP: rs121912726
rs121912726
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0268389
Disease:
Amyloidosis, familial visceral 		G 0.700 CausalMutation CLINVAR
dbSNP: rs121912729
rs121912729
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0268389
Disease:
Amyloidosis, familial visceral 		G 0.700 CausalMutation CLINVAR
dbSNP: rs121912730
rs121912730
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0268389
Disease:
Amyloidosis, familial visceral 		G 0.700 CausalMutation CLINVAR