ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.1738-10T>C

dbSNP: rs2147171593
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002162028 SCV002336606 likely benign Neurofibromatosis, type 2 2022-02-18 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV002162028 SCV004832788 likely benign Neurofibromatosis, type 2 2023-06-26 criteria provided, single submitter clinical testing

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