ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.960A>G (p.Leu320=) (rs56093012)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000323678 SCV000338428 uncertain significance not provided 2016-01-26 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001289913 SCV001477915 likely benign none provided 2020-05-29 criteria provided, single submitter clinical testing

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