ClinVar Miner

Submissions for variant NM_012472.6(DNAAF11):c.1392G>A (p.Pro464=)

dbSNP: rs146460901
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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 RCV003538963 SCV004281966 benign Primary ciliary dyskinesia 19 2024-10-19 criteria provided, single submitter clinical testing

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