ClinVar Miner

Submissions for variant NM_022051.3(EGLN1):c.1012-14G>C

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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 RCV003612028 SCV004523851 likely benign Erythrocytosis, familial, 3 2024-12-19 criteria provided, single submitter clinical testing

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