ClinVar Miner

Submissions for variant NM_005188.3(CBL):c.869+19A>G (rs181589369)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000049225 SCV000077239 benign Rasopathy 2012-04-02 criteria provided, single submitter clinical testing The variant is found in NOONAN panel(s).
PreventionGenetics RCV000250922 SCV000310879 benign not specified criteria provided, single submitter clinical testing

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