ClinVar Miner

Submissions for variant NM_017565.4(FAM20A):c.1091C>T (p.Thr364Ile)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005022571 SCV005651027 uncertain significance Amelogenesis imperfecta type 1G 2024-04-20 criteria provided, single submitter clinical testing

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