ClinVar Miner

Submissions for variant NM_001369.3(DNAH5):c.11570+35A>G

gnomAD frequency: 0.57196  dbSNP: rs3734109
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000253687 SCV000307674 benign not specified criteria provided, single submitter clinical testing
Pars Genome Lab RCV001527512 SCV001738559 benign Primary ciliary dyskinesia 3 2021-06-15 criteria provided, single submitter clinical testing
GeneDx RCV001689826 SCV001909226 benign not provided 2019-04-04 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001689826 SCV005305996 benign not provided criteria provided, single submitter not provided

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