ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.3530del (p.Lys1177fs) (rs397508579)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000757086 SCV000885190 pathogenic not provided 2017-10-23 criteria provided, single submitter clinical testing
ClinVar Staff, National Center for Biotechnology Information (NCBI) RCV000577604 SCV000679382 not provided Cystic fibrosis no assertion provided literature only

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