| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Deafness_IsolatedAndComplex v1.294 | MYO1C | Chirag Patel Marked gene: MYO1C as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.294 | MYO1C | Chirag Patel Gene: myo1c has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.293 | MYO1C |
Chirag Patel gene: MYO1C was added gene: MYO1C was added to Deafness_IsolatedAndComplex. Sources: ClinGen disputed tags were added to gene: MYO1C. Mode of inheritance for gene: MYO1C was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: MYO1C were set to Nonsyndromic genetic hearing loss, MONDO:0019497 Review for gene: MYO1C was set to RED Added comment: ClinGen DISPUTED - Jun 2018 Sources: ClinGen |
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