ClinVar Miner

Submissions for variant NM_001206927.2(DNAH8):c.7569G>A (p.Lys2523=)

gnomAD frequency: 0.42138  dbSNP: rs9380795
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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 RCV000455873 SCV000538979 benign not specified 2016-03-28 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
Invitae RCV001520278 SCV001729340 benign Primary ciliary dyskinesia 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001712407 SCV001939081 benign not provided 2018-11-10 criteria provided, single submitter clinical testing

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