Variant: rs9822953 

    present in Gene: LINC00886
    present in Chromosome: 3
    Position on Chromosome: 156754282
    Alleles of this Variant: C/G;T

rs9822953 in LINC00886 gene and Central corneal thickness PMID 29760442 2018 Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.

rs9822953 in LINC00886 gene and Corneal Topography PMID 23291589 2013 Genome-wide association analyses identify multiple loci associated with central corneal thickness and keratoconus.