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Fetal anomalies v0.2522 | WNT3 | Zornitza Stark Marked gene: WNT3 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Fetal anomalies v0.2522 | WNT3 | Zornitza Stark Gene: wnt3 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Fetal anomalies v0.2522 | WNT3 | Zornitza Stark Phenotypes for gene: WNT3 were changed from TETRA-AMELIA SYNDROME to Tetra-amelia syndrome 1, OMIM #273395 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Fetal anomalies v0.2001 | WNT3 | Chirag Patel Classified gene: WNT3 as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Fetal anomalies v0.2001 | WNT3 | Chirag Patel Gene: wnt3 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Fetal anomalies v0.2000 | WNT3 | Chirag Patel reviewed gene: WNT3: Rating: RED; Mode of pathogenicity: None; Publications: PubMed: 14872406; Phenotypes: ?Tetra-amelia syndrome 1, OMIM #273395; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Fetal anomalies v0.0 | WNT3 |
Zornitza Stark gene: WNT3 was added gene: WNT3 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: WNT3 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: WNT3 were set to 18837045; 16283889; 14872406 Phenotypes for gene: WNT3 were set to TETRA-AMELIA SYNDROME |