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| Rare syndromic craniosynostosis or isolated multisuture synostosis v1.72 | KRAS | Eleanor Williams Added phenotypes Noonan syndrome type 3 609942; cardiofaciocutaneous syndrome type 2 615278 for gene: KRAS | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rare syndromic craniosynostosis or isolated multisuture synostosis v1.47 | KRAS | Tracy Lester reviewed gene: KRAS: Rating: GREEN; Mode of pathogenicity: Loss-of-function variants (as defined in pop up message) DO NOT cause this phenotype - please provide details in the comments; Publications: 19396835, 22488932; Phenotypes: Noonan syndrome type 3 - 609942, cardiofaciocutaneous syndrome type 2 - 615278; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rare syndromic craniosynostosis or isolated multisuture synostosis v1.46 | KRAS | Eleanor Williams reviewed gene: KRAS: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Rare syndromic craniosynostosis or isolated multisuture synostosis v1.45 | KRAS |
Eleanor Williams Source NHS GMS was added to KRAS. Rating Changed from Green List (high evidence) to Green List (high evidence) |
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