ClinVar Miner

Submissions for variant NM_022051.3(EGLN1):c.1217-10del

dbSNP: rs371155853
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000327516 SCV000355509 benign Familial erythrocytosis 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001618508 SCV001847578 benign not provided 2019-08-15 criteria provided, single submitter clinical testing

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