ClinVar Miner

Submissions for variant NM_000267.3(NF1):c.1974C>A (p.Leu658=) (rs751318331)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000219277 SCV000278002 likely benign Hereditary cancer-predisposing syndrome 2015-08-25 criteria provided, single submitter clinical testing
Invitae RCV000632576 SCV000753761 likely benign Neurofibromatosis, type 1 2017-12-15 criteria provided, single submitter clinical testing
PreventionGenetics RCV000242668 SCV000306243 likely benign not specified criteria provided, single submitter clinical testing

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