ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.870-1G>C (rs1351058559)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000670583 SCV000795452 likely pathogenic Cystic fibrosis 2017-11-08 criteria provided, single submitter clinical testing
Baylor Genetics RCV001004241 SCV001163117 pathogenic Cystic fibrosis; Congenital bilateral aplasia of vas deferens from CFTR mutation criteria provided, single submitter clinical testing

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