Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61748436
rs61748436
CRX
0.710 GeneticVariation UNIPROT Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies. 11139241

2001
dbSNP: rs61748436
rs61748436
CRX
0.710 GeneticVariation BEFREE We also found a previously reported missense mutation, Arg41Gln, heterozygously in a 47-year-old patient with a form of RP. 11748859

2001
dbSNP: rs61748436
rs61748436
CRX
0.710 GeneticVariation UNIPROT A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene. 9792858

1998
dbSNP: rs61748436
rs61748436
CRX
0.710 GeneticVariation UNIPROT Mutations in the cone-rod homeobox gene are associated with the cone-rod dystrophy photoreceptor degeneration. 9427255

1997