ClinVar Miner

Submissions for variant NM_001369.3(DNAH5):c.6989-18T>C

dbSNP: rs2151800885
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Pars Genome Lab RCV001527533 SCV001738607 likely benign Primary ciliary dyskinesia 3 2021-06-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003538805 SCV004344530 likely benign Primary ciliary dyskinesia 2023-07-25 criteria provided, single submitter clinical testing

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