ClinVar Miner

Submissions for variant NM_022051.3(EGLN1):c.891+17G>A

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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 RCV002599559 SCV003498950 likely benign Erythrocytosis, familial, 3 2023-06-25 criteria provided, single submitter clinical testing

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