ClinVar Miner

Submissions for variant NM_018076.5(ODAD2):c.1797G>A (p.Leu599=)

dbSNP: rs926907910
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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 RCV001402581 SCV001604432 likely benign Primary ciliary dyskinesia 23 2021-01-15 criteria provided, single submitter clinical testing

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