ClinVar Miner

Submissions for variant NM_001277115.2(DNAH11):c.8798-36T>C

gnomAD frequency: 0.01196  dbSNP: rs115125824
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001596060 SCV001828010 likely benign not provided 2019-05-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001596060 SCV005224634 likely benign not provided criteria provided, single submitter not provided

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