ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.3718-24G>A (rs374013084)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000594601 SCV000705210 uncertain significance not provided 2017-01-03 criteria provided, single submitter clinical testing
Invitae RCV001085769 SCV001001991 benign Cystic fibrosis 2019-12-31 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000594601 SCV001134143 uncertain significance not provided 2019-08-14 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001001722 SCV001159307 likely benign not specified 2019-04-15 criteria provided, single submitter clinical testing

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