ClinVar Miner

Submissions for variant NM_001206927.2(DNAH8):c.13054-17T>C

gnomAD frequency: 0.40469  dbSNP: rs3737095
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Preventiongenetics, part of Exact Sciences RCV000248148 SCV000307049 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001640510 SCV001859312 benign not provided 2018-11-11 criteria provided, single submitter clinical testing
Invitae RCV002057990 SCV002410865 benign Primary ciliary dyskinesia 2024-01-31 criteria provided, single submitter clinical testing

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