| Date | Panel | Item | Activity | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Deafness_IsolatedAndComplex v1.294 | GJA1 | Chirag Patel Marked gene: GJA1 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.294 | GJA1 | Chirag Patel Gene: gja1 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Deafness_IsolatedAndComplex v1.292 | GJA1 |
Chirag Patel gene: GJA1 was added gene: GJA1 was added to Deafness_IsolatedAndComplex. Sources: ClinGen disputed tags were added to gene: GJA1. Mode of inheritance for gene: GJA1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: GJA1 were set to Nonsyndromic genetic hearing loss, MONDO:0019497 Review for gene: GJA1 was set to RED Added comment: ClinGen DISPUTED - Mar 2022 Sources: ClinGen |
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