APOA5, apolipoprotein A5, 116519

N. diseases: 107; N. variants: 22
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs651821
rs651821
Entrez Id: 116519
Gene Symbol: APOA5
APOA5
CUI: C0524620
Disease:
Metabolic Syndrome X
C 0.720 GeneticVariation GWASCAT Notably, by an integrated analysis of the genotypes and the serum levels of APOA5, BUD13 and triglyceride, we observed that BUD13 was another potential mediator, besides APOA5, of the association between rs651821 and serum triglyceride. rs671 (ALDH2), an east Asian-specific common variant, was found to be associated with MetS (P<sub>combined</sub> = 9.7 × 10<sup>-22</sup> ) in Han Chinese. 28371326 2017
dbSNP: rs651821
rs651821
Entrez Id: 116519
Gene Symbol: APOA5
APOA5
CUI: C0524620
Disease:
Metabolic Syndrome X
0.720 GeneticVariation BEFREE Even after adjustment for MetS status, reduced abundances of Actinobacteria and <i>Bifidobacterium</i> were significantly linked to the minor allele at the <i>APOA5</i> SNP rs651821. 27053630 2017
dbSNP: rs651821
rs651821
Entrez Id: 116519
Gene Symbol: APOA5
APOA5
CUI: C0524620
Disease:
Metabolic Syndrome X
0.720 GeneticVariation BEFREE Notably, by an integrated analysis of the genotypes and the serum levels of APOA5, BUD13 and triglyceride, we observed that BUD13 was another potential mediator, besides APOA5, of the association between rs651821 and serum triglyceride. rs671 (ALDH2), an east Asian-specific common variant, was found to be associated with MetS (P<sub>combined</sub> = 9.7 × 10<sup>-22</sup> ) in Han Chinese. 28371326 2017