Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3135506
rs3135506
Entrez Id: 116519
Gene Symbol: APOA5
APOA5
CUI: C1956346
Disease:
Coronary Artery Disease
0.050 GeneticVariation BEFREE Mediation analysis yielded a mediation effect of p.S19W on risk of premature CAD through HDL-C (OR = 0.98, P = 0.040) and TG (OR = 0.98, P = 0.042), suggesting a causal relationship between p.S19W and premature CAD partially through its effects on HDL-C and TG levels. 30024021 2018
dbSNP: rs3135506
rs3135506
Entrez Id: 116519
Gene Symbol: APOA5
APOA5
CUI: C1956346
Disease:
Coronary Artery Disease
0.050 GeneticVariation BEFREE The genetic variants of rs3135506 (G), rs10455872 (A) and rs3798220 (G) have low frequency in our population and reflected no association with CAD. 29309886 2018
dbSNP: rs3135506
rs3135506
Entrez Id: 116519
Gene Symbol: APOA5
APOA5
CUI: C1956346
Disease:
Coronary Artery Disease
0.050 GeneticVariation BEFREE From these data, we conclude that (1) APOA5 p.S19W is a common variant, with very few additional APOA5 gene mutations; (2) APOA5 p.S19W plays a major role in triglyceride metabolism; and (3) APOA5 p.S19W is a CAD risk factor. 22914599 2012
dbSNP: rs3135506
rs3135506
Entrez Id: 116519
Gene Symbol: APOA5
APOA5
CUI: C1956346
Disease:
Coronary Artery Disease
0.050 GeneticVariation BEFREE Therefore, the present study aimed to elucidate the relationship of four single nucleotide polymorphisms (SNPs) in the Apo11q cluster, namely the -75G>A, +83C>T SNPs in the APOA1 gene, the Sac1 SNP in the APOC3 gene and the S19W variant in the APOA5 gene to plasma lipids and CAD in 190 affected sibling pairs (ASPs) belonging to Asian Indian families with a strong CAD history. 18801202 2008
dbSNP: rs3135506
rs3135506
Entrez Id: 116519
Gene Symbol: APOA5
APOA5
CUI: C1956346
Disease:
Coronary Artery Disease
0.050 GeneticVariation BEFREE Nine hundred and thirteen angiografically defined patients (669 CAD and 244 CAD-free) were genotyped for APOA5 -1131 C>T and S19W polymorphisms. 16682041 2007