ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.744-33GATT[6] (rs1805171)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory for Molecular Medicine, Partners HealthCare Personalized Medicine RCV000036521 SCV000060176 benign not specified 2011-10-20 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000036521 SCV000304502 benign not specified criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000036521 SCV000602971 benign not specified 2018-07-01 criteria provided, single submitter clinical testing
CFTR-France RCV001009355 SCV001169208 benign Cystic fibrosis 2018-01-29 criteria provided, single submitter curation the variant does not result in CFTR-RD neither

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