Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs662799
rs662799
CUI: C0020473
Disease: Hyperlipidemia
Hyperlipidemia
0.010 GeneticVariation BEFREE Excess risk for low HDL-C and hyperlipidemia was associated with rs662799 genotype alleles of APOA5 SNPs in older Chinese adults. 29758349

2018