ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.11952C>T (p.His3984=)

dbSNP: rs1368615388
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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 RCV003651430 SCV004529907 likely benign Primary ciliary dyskinesia 2024-03-16 criteria provided, single submitter clinical testing

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