ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.11203-4C>T

gnomAD frequency: 0.00088  dbSNP: rs200188856
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000246159 SCV000307429 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV000476346 SCV000561963 likely benign Primary ciliary dyskinesia 2024-01-29 criteria provided, single submitter clinical testing

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