Gene: APOA1 ×
Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1264352930
rs1264352930
APOA1 ; APOA1-AS
0.010 GeneticVariation BEFREE Delayed postprandial retinyl palmitate and squalene removal in a patient heterozygous for apolipoprotein A-IFIN mutation (Leu 159-->Arg) and low HDL cholesterol level without coronary artery disease. 9125314

1996
dbSNP: rs1384889210
rs1384889210
APOA1 ; APOA1-AS
0.010 GeneticVariation BEFREE Compound heterozygosity for a structural apolipoprotein A-I variant, apo A-I(L141R)Pisa, and an apolipoprotein A-I null allele in patients with absence of HDL cholesterol, corneal opacifications, and coronary heart disease. 8840853

1996