ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.3139+8A>G (rs193922517)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Integrated Genetics/Laboratory Corporation of America RCV000029518 SCV000052169 uncertain Cystic fibrosis 2011-08-18 criteria provided, single submitter clinical testing Converted during submission to Uncertain significance.
Counsyl RCV000029518 SCV000791780 uncertain significance Cystic fibrosis 2017-05-23 criteria provided, single submitter clinical testing
Invitae RCV000029518 SCV001000951 likely benign Cystic fibrosis 2019-12-31 criteria provided, single submitter clinical testing

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