Albinism or congenital nystagmus Gene Set

Dataset	ClinVar Gene-Phenotype Associations 2025
Category	disease or phenotype associations
Type	phenotype
External Link	https://www.ncbi.nlm.nih.gov/medgen/C0950123
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Genes

4 genes associated with the Albinism or congenital nystagmus phenotype from the curated ClinVar Gene-Phenotype Associations 2025 dataset.

Symbol	Name
OCA2	oculocutaneous albinism II
PAX6	paired box 6
SLC45A2	solute carrier family 45, member 2
TYR	tyrosinase