ClinVar Miner

Submissions for variant NM_001369.3(DNAH5):c.3397-51T>C

gnomAD frequency: 0.42101  dbSNP: rs10513159
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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 RCV001527590 SCV001738695 benign Primary ciliary dyskinesia 3 2021-06-15 criteria provided, single submitter clinical testing
GeneDx RCV001712958 SCV001942371 benign not provided 2018-11-11 criteria provided, single submitter clinical testing

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