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Retinal disorders v2.209 | LRP1 | Ivone Leong Classified gene: LRP1 as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Retinal disorders v2.209 | LRP1 | Ivone Leong Added comment: Comment on list classification: New gene added by Zornitza Stark (Australian Genomics). This gene is not associated with a phenotype in OMIM or Gene2Phenotype. There is currently not enough evidence to support a gene-disease association. This gene has been given a Red rating. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Retinal disorders v2.209 | LRP1 | Ivone Leong Gene: lrp1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Retinal disorders v2.208 | LRP1 |
Zornitza Stark gene: LRP1 was added gene: LRP1 was added to Retinal disorders. Sources: Literature Mode of inheritance for gene: LRP1 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: LRP1 were set to 33776059 Phenotypes for gene: LRP1 were set to Macular drusen Review for gene: LRP1 was set to RED Added comment: PMID: 33776059 - 2x unrelated individuals with compound heterozygous missense variants and inherited retinal disorder/macular drusen. No functional data. Sources: Literature |