Variant: rs369484186 

    present in Gene: LOC105370752;TRPM1
    present in Chromosome: 15
    Position on Chromosome: 31031040
    Alleles of this Variant: T/A

rs369484186 in LOC105370752;TRPM1 gene and NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C PMID 19878917 2009 Recessive mutations of the gene TRPM1 abrogate ON bipolar cell function and cause complete congenital stationary night blindness in humans.

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

PMID 19896109 2009 Mutations in TRPM1 are a common cause of complete congenital stationary night blindness.