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| Mendeliome v1.2629 | PTPRB | Bryony Thompson Marked gene: PTPRB as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v1.2629 | PTPRB | Bryony Thompson Gene: ptprb has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mendeliome v1.2629 | PTPRB |
Bryony Thompson gene: PTPRB was added gene: PTPRB was added to Mendeliome. Sources: Literature Mode of inheritance for gene: PTPRB was set to Unknown Publications for gene: PTPRB were set to 40319023 Phenotypes for gene: PTPRB were set to central serous chorioretinopathy; varicose veins; glaucoma Review for gene: PTPRB was set to RED Added comment: A single risk allele (rs113791087 - missense) associated with the risk of central serous chorioretinopathy, varicose veins and glaucoma (reduced risk). Not associated with Mendelian disease. Sources: Literature |
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