ClinVar Miner

Submissions for variant NM_001206927.2(DNAH8):c.12008-8T>C

gnomAD frequency: 0.00019  dbSNP: rs772870720
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000865899 SCV001006926 likely benign Primary ciliary dyskinesia 2024-09-15 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004705822 SCV005223745 likely benign not provided criteria provided, single submitter not provided

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