ClinVar Miner

Submissions for variant NM_022051.3(EGLN1):c.891+8T>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 RCV003612559 SCV004402494 likely benign Erythrocytosis, familial, 3 2023-05-16 criteria provided, single submitter clinical testing

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