ClinVar Miner

Submissions for variant NM_001010892.3(RSPH4A):c.687-20A>C

dbSNP: rs773538494
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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 RCV002187885 SCV002354868 likely benign Primary ciliary dyskinesia 2021-07-03 criteria provided, single submitter clinical testing

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