ClinVar Miner

Submissions for variant NM_000479.5(AMH):c.1015dup (p.Leu339fs)

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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 RCV005026446 SCV005648228 likely pathogenic Persistent Mullerian duct syndrome 2024-05-24 criteria provided, single submitter clinical testing

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