Variant: rs121908190 

    present in Gene: C1QTNF5;MFRP
    present in Chromosome: 11
    Position on Chromosome: 119345516
    Alleles of this Variant: A/G

rs121908190 in C1QTNF5;MFRP gene and NANOPHTHALMOS 2 (disorder) PMID 15976030 2005 Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein.