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| Skeletal dysplasia v0.324 | DNMT3A | Chirag Patel Publications for gene DNMT3A were changed from 24614070 to 24614070 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Skeletal dysplasia v0.323 | DNMT3A |
Chirag Patel Source Victorian Clinical Genetics Services was removed from DNMT3A. Phenotypes for gene: DNMT3A were changed from Tatton-Brown-Rahman syndrome 615879 to Heyn-Sproul-Jackson syndrome, MIM# 618724 |
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| Skeletal dysplasia v0.3 | DNMT3A | Sue White reviewed gene: DNMT3A: Rating: GREEN; Mode of pathogenicity: None; Publications: 24614070, 30478443; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Skeletal dysplasia v0.0 | DNMT3A |
Zornitza Stark gene: DNMT3A was added gene: DNMT3A was added to Skeletal dysplasia. Sources: NHS GMS,Expert list,Expert Review Green Mode of inheritance for gene: DNMT3A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: DNMT3A were set to Tatton-Brown-Rahman syndrome 615879 |
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