Variant: rs538509310 

    present in Gene: SNHG22
    present in Chromosome: 18
    Position on Chromosome: 49817040
    Alleles of this Variant: T/A

rs538509310 in SNHG22 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.

rs538509310 in SNHG22 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.