ClinVar Miner

Submissions for variant NM_199334.5(THRA):c.814G>A (p.Asp272Asn)

dbSNP: rs2145085076
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Molecular Genetics (Pr. Bezieau's lab), CHU de Nantes RCV001780020 SCV002016263 uncertain significance Neurodevelopmental disorder 2021-06-21 criteria provided, single submitter clinical testing

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