Variant: rs869312176 

    present in Gene: TRPM1;MIR211
    present in Chromosome: 15
    Position on Chromosome: 31066093
    Alleles of this Variant: A/G

rs869312176 in TRPM1;MIR211 gene and NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C PMID 26872967 2016 Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease.