ClinVar Miner

Submissions for variant NM_173628.4(DNAH17):c.4584+13C>T

gnomAD frequency: 0.31368  dbSNP: rs9894913
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine RCV000454522 SCV000538897 benign not specified 2016-03-29 criteria provided, single submitter clinical testing Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: Frequency
GeneDx RCV001709647 SCV001936797 benign not provided 2021-05-11 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001709647 SCV005255125 benign not provided criteria provided, single submitter not provided

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