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| Congenital nystagmus v0.23 | CNGB3 | Zornitza Stark Marked gene: CNGB3 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital nystagmus v0.23 | CNGB3 | Zornitza Stark Gene: cngb3 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital nystagmus v0.23 | CNGB3 | Zornitza Stark changed review comment from: Well established gene-disease association. The c.1148delC is a common founder variant in the Pingelapese.; to: Well established gene-disease association. The c.1148delC is a common founder variant in the Pingelapese. Nystagmus is a feature. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Congenital nystagmus v0.4 | CNGB3 |
Zornitza Stark gene: CNGB3 was added gene: CNGB3 was added to Congenital nystagmus. Sources: Expert Review Green,Expert list Mode of inheritance for gene: CNGB3 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: CNGB3 were set to 17265047 Phenotypes for gene: CNGB3 were set to Achromatopsia 3 MIM#262300 |
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