Variant: rs122456134 

    present in Gene: CACNA1F
    present in Chromosome: X
    Position on Chromosome: 49218511
    Alleles of this Variant: G/A

rs122456134 in CACNA1F gene and Night blindness, congenital stationary PMID 9662399 1998 An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.