ClinVar Miner

Submissions for variant NM_000240.4(MAOA):c.156A>G (p.Thr52=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005123438 SCV005740528 likely benign Brunner syndrome 2024-03-31 criteria provided, single submitter clinical testing

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