ClinVar Miner

Submissions for variant NM_000492.4(CFTR):c.3874-14C>G

gnomAD frequency: 0.00001  dbSNP: rs184271150
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000669170 SCV000793892 uncertain significance Cystic fibrosis 2017-09-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000669170 SCV002373154 likely benign Cystic fibrosis 2023-12-14 criteria provided, single submitter clinical testing

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