ClinVar Miner

Submissions for variant NM_173628.4(DNAH17):c.5322+8C>T

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003421524 SCV004144386 likely benign not provided 2023-01-01 criteria provided, single submitter clinical testing DNAH17: BP4, BS2
PreventionGenetics, part of Exact Sciences RCV003938954 SCV004749498 benign DNAH17-related disorder 2019-06-24 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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