Variant: rs61748436 

    present in Gene: CRX
    present in Chromosome: 19
    Position on Chromosome: 47836264
    Alleles of this Variant: G/A

rs61748436 in CRX gene and Retinitis Pigmentosa PMID 9427255 1997 Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration.

PMID 9792858 1998 A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene.

PMID 11139241 2001 Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies.