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| Structural eye disease v1.123 | FANCL | Arina Puzriakova Mode of inheritance for gene: FANCL was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.91 | FANCL | Nicola Ragge reviewed gene: FANCL: Rating: AMBER; Mode of pathogenicity: ; Publications: 25754594; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.89 | FANCL |
Ivone Leong Source NHS GMS was added to FANCL. Publications for gene FANCL were changed from to 25754594 |
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| Structural eye disease v0.88 | FANCL |
Ivone Leong Source Expert Review Amber was added to FANCL. Rating Changed from Red List (low evidence) to Amber List (moderate evidence) |
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| Structural eye disease v0.60 | FANCL | Mariya Moosajee reviewed gene: FANCL: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Fanconi Anemia, Complementation Group L, FANCL; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.59 | FANCL |
Ivone Leong gene: FANCL was added gene: FANCL was added to Structural eye disease. Sources: London North GLH Mode of inheritance for gene: FANCL was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: FANCL were set to Fanconi Anemia, Complementation Group L, FANCL, 614083 |
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