ClinVar Miner

Submissions for variant NM_000492.4(CFTR):c.2620-97C>T

gnomAD frequency: 0.00011  dbSNP: rs146376436
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000665665 SCV000789823 uncertain significance Cystic fibrosis 2017-02-22 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000665665 SCV001702195 likely benign Cystic fibrosis 2022-11-23 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV003736877 SCV004565253 likely benign not provided 2023-03-22 criteria provided, single submitter clinical testing

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