ClinVar Miner

Submissions for variant NM_000492.4(CFTR):c.3184C>T (p.Leu1062=)

dbSNP: rs2485130273
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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 RCV003617383 SCV004448606 likely benign Cystic fibrosis 2023-03-14 criteria provided, single submitter clinical testing

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