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| Fetal anomalies v0.3766 | SLC26A7 | Zornitza Stark Marked gene: SLC26A7 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v0.3766 | SLC26A7 | Zornitza Stark Gene: slc26a7 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v0.3766 | SLC26A7 | Zornitza Stark Classified gene: SLC26A7 as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v0.3766 | SLC26A7 | Zornitza Stark Gene: slc26a7 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v0.3765 | SLC26A7 | Zornitza Stark reviewed gene: SLC26A7: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v0.3721 | SLC26A7 |
Krithika Murali gene: SLC26A7 was added gene: SLC26A7 was added to Fetal anomalies. Sources: Literature Mode of inheritance for gene: SLC26A7 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: SLC26A7 were set to 34780050; 32486989; 31372509; 30333321; 29546359 Phenotypes for gene: SLC26A7 were set to Thyroid dyshormogenesis - no OMIM gene disease association Review for gene: SLC26A7 was set to GREEN Added comment: Biallelic variants associated with congenital hypothyroidism secondary to thyroid dyshormogenesis. PMID 32486989 report an affected female diagnosed with goitre D4 of life. Sources: Literature |
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