Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894459
rs104894459
Entrez Id: 4901
Gene Symbol: NRL
NRL
CUI: C0035334
Disease:
Retinitis Pigmentosa
0.010 GeneticVariation BEFREE Phenotype of retinitis pigmentosa associated with the Ser50Thr mutation in the NRL gene. 12796249 2003