ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.2475C>T (p.Asn825=) (rs746961486)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000759037 SCV000625736 likely benign not provided 2019-01-31 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000759037 SCV000888079 likely benign not provided 2019-05-16 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV001001352 SCV001158547 likely benign not specified 2019-06-21 criteria provided, single submitter clinical testing

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