ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.1743C>T (p.Thr581=)

dbSNP: rs768807694
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001499407 SCV001704171 likely benign Neurofibromatosis, type 2 2023-05-19 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV001499407 SCV004838190 likely benign Neurofibromatosis, type 2 2023-11-20 criteria provided, single submitter clinical testing

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