ClinVar Miner

Submissions for variant NM_018076.5(ODAD2):c.2946G>T (p.Ala982=)

dbSNP: rs371338930
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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 RCV001493066 SCV001697688 likely benign Primary ciliary dyskinesia 23 2022-08-09 criteria provided, single submitter clinical testing

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