Variant: rs11139399 

    present in Gene: LOC101927502
    present in Chromosome: 9
    Position on Chromosome: 81757826
    Alleles of this Variant: T/C

rs11139399 in LOC101927502 gene and Hippocampal atrophy PMID 22745009 2012 Multiple loci influencing hippocampal degeneration identified by genome scan.

rs11139399 in LOC101927502 gene and Serum albumin measurement PMID 23281178 2013 A genome-wide assessment of variability in human serum metabolism.