Variant: rs11626056 

    present in Gene: LOC101927598
    present in Chromosome: 14
    Position on Chromosome: 51766558
    Alleles of this Variant: C/T

rs11626056 in LOC101927598 gene and Hippocampal atrophy PMID 19668339 2009 Hippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's disease.