ClinVar Miner

Submissions for variant NM_000240.4(MAOA):c.1263-16C>G

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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 RCV002900218 SCV003251325 benign Brunner syndrome 2024-12-09 criteria provided, single submitter clinical testing

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