ClinVar Miner

Submissions for variant NM_023036.6(DNAI2):c.114C>G (p.Ala38=)

dbSNP: rs763489979
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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 RCV001501187 SCV001705993 likely benign Primary ciliary dyskinesia 2022-09-02 criteria provided, single submitter clinical testing

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