ClinVar Miner

Submissions for variant NM_001369.3(DNAH5):c.5115-49G>C

dbSNP: rs10041099
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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 RCV000254063 SCV000307780 benign not specified criteria provided, single submitter clinical testing
Pars Genome Lab RCV001527547 SCV001738633 benign Primary ciliary dyskinesia 3 2021-06-15 criteria provided, single submitter clinical testing
GeneDx RCV001683022 SCV001900662 benign not provided 2018-11-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001683022 SCV005306036 benign not provided criteria provided, single submitter not provided

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