ClinVar Miner

Submissions for variant NM_000492.4(CFTR):c.2989-6T>C

dbSNP: rs2485128868
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003618373 SCV004407572 likely benign Cystic fibrosis 2022-10-27 criteria provided, single submitter clinical testing

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