Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1264352930
rs1264352930
Entrez Id: 335;104326055
Gene Symbol: APOA1;APOA1-AS
APOA1;APOA1-AS
CUI: C0473527
Disease:
Hypoalphalipoproteinemias
0.010 GeneticVariation BEFREE We have devised a combined in vivo, ex vivo, and in vitro approach to elucidate the mechanism(s) responsible for the hypoalphalipoproteinemia in heterozygous carriers of a naturally occurring apolipoprotein A-I (apoA-I) variant (Leu(159) to Arg) known as apoA-I Finland (apoA-I(FIN)). 11292828 2001