Variant: rs770066665 

    present in Gene: GPR179
    present in Chromosome: 17
    Position on Chromosome: 38337640
    Alleles of this Variant: G/-

rs770066665 in GPR179 gene and Night blindness, congenital stationary PMID 22325362 2012 GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.

PMID 22325361 2012 Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.