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| Structural eye disease v0.76 | KCNV2 | Nicola Ragge reviewed gene: KCNV2: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinal cone dystrophy 3B, 610356; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.38 | KCNV2 | Ivone Leong reviewed gene: KCNV2: Rating: RED; Mode of pathogenicity: ; Publications: ; Phenotypes: Retinal cone dystrophy 3B, 610356; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Structural eye disease v0.15 | KCNV2 |
Ivone Leong Source NHS GMS was added to KCNV2. Mode of inheritance for gene KCNV2 was changed from to BIALLELIC, autosomal or pseudoautosomal Added phenotypes Retinal cone dystrophy 3B, 610356 for gene: KCNV2 |
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| Structural eye disease v0.2 | KCNV2 |
Ellen McDonagh gene: KCNV2 was added gene: KCNV2 was added to Structural eye disease. Sources: Expert Review Red Mode of inheritance for gene: KCNV2 was set to Phenotypes for gene: KCNV2 were set to Eye Disorders |
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