ClinVar Miner

Submissions for variant NM_001247997.2(CLIP1):c.297C>T (p.Asn99=)

gnomAD frequency: 0.00127  dbSNP: rs141383610
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV000502621 SCV000594146 likely benign not specified 2016-06-02 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000933263 SCV001078957 benign not provided 2018-07-13 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003925454 SCV004746954 likely benign CLIP1-related disorder 2019-10-28 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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