Variant: rs140039128 

    present in Gene: LOC105371046;IFT140
    present in Chromosome: 16
    Position on Chromosome: 1583369
    Alleles of this Variant: C/T

rs140039128 in LOC105371046;IFT140 gene and Mainzer-Saldino Disease PMID 26216056 2015 Mutations in human IFT140 cause non-syndromic retinal degeneration.