ClinVar Miner

Submissions for variant NM_000492.3(CFTR):c.3717+45G>A (rs145743767)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000591755 SCV000709661 benign not specified 2017-06-29 criteria provided, single submitter clinical testing
ClinVar Staff, National Center for Biotechnology Information (NCBI) RCV000577129 SCV000679446 not provided Cystic fibrosis no assertion provided literature only

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