ClinVar Miner

Submissions for variant NM_001386125.1(OBSCN):c.2172G>A (p.Ala724=)

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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 RCV005162497 SCV005783846 benign not provided 2025-01-27 criteria provided, single submitter clinical testing

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