ClinVar Miner

Submissions for variant NM_001369.3(DNAH5):c.10102-29C>T

gnomAD frequency: 0.30675  dbSNP: rs6554813
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000245619 SCV000307658 benign not specified criteria provided, single submitter clinical testing
Pars Genome Lab RCV001527530 SCV001738600 benign Primary ciliary dyskinesia 3 2021-06-15 criteria provided, single submitter clinical testing
GeneDx RCV001618415 SCV001843964 benign not provided 2018-11-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001527530 SCV001875592 benign Primary ciliary dyskinesia 3 2021-07-30 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001618415 SCV005306001 benign not provided criteria provided, single submitter not provided

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