ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.1431C>G (p.Thr477=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
All of Us Research Program, National Institutes of Health RCV004013603 SCV004829789 likely benign Neurofibromatosis, type 2 2023-08-08 criteria provided, single submitter clinical testing

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