ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.2736G>A (p.Ser912=) (rs200901072)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000175142 SCV000226577 uncertain significance not provided 2014-12-23 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001290670 SCV001478798 likely benign not specified 2021-01-22 criteria provided, single submitter clinical testing
Invitae RCV001409458 SCV001611481 likely benign Cystic fibrosis 2020-12-04 criteria provided, single submitter clinical testing

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