ClinVar Miner

Submissions for variant NM_182943.3(PLOD2):c.338+12A>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 RCV005130129 SCV005749577 likely benign not provided 2024-04-08 criteria provided, single submitter clinical testing

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