Variant: rs150441866 

    present in Gene: TRPM1
    present in Chromosome: 15
    Position on Chromosome: 31069884
    Alleles of this Variant: A/C

rs150441866 in TRPM1 gene and NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C PMID 20300565 2010 TRPM1 mutations are associated with the complete form of congenital stationary night blindness.

PMID 19896113 2009 TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.