ClinVar Miner

Submissions for variant NM_018139.2(DNAAF2):c.707C>T (p.Pro236Leu) (rs74050429)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000204122 SCV000386862 likely benign Primary ciliary dyskinesia 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000204122 SCV000262497 benign Primary ciliary dyskinesia 2018-01-03 criteria provided, single submitter clinical testing
PreventionGenetics RCV000245254 SCV000313205 benign not specified criteria provided, single submitter clinical testing

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