Variant: rs768116521 

    present in Gene: LOC105372112
    present in Chromosome: 18
    Position on Chromosome: 49629266
    Alleles of this Variant: G/A;T

rs768116521 in LOC105372112 gene and High density lipoprotein measurement PMID 29084231 2017 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.

rs768116521 in LOC105372112 gene and Phospholipid measurement PMID 29084231 2017 Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.