ClinVar Miner

Submissions for variant NM_001440.4(EXTL3):c.1686A>C (p.Gly562=)

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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 RCV005149520 SCV005780365 likely benign not provided 2024-05-26 criteria provided, single submitter clinical testing

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