ClinVar Miner

Submissions for variant NM_001256715.2(DNAAF3):c.323-17T>G

gnomAD frequency: 0.01106  dbSNP: rs10407660
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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 RCV000254208 SCV000307136 benign not specified criteria provided, single submitter clinical testing
Eurofins Ntd Llc (ga) RCV000254208 SCV000342409 benign not specified 2016-06-13 criteria provided, single submitter clinical testing
GeneDx RCV001561637 SCV001784272 likely benign not provided 2019-09-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002057999 SCV002401807 benign Primary ciliary dyskinesia 2025-01-08 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001561637 SCV005206066 likely benign not provided criteria provided, single submitter not provided

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