ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.676-12T>C

gnomAD frequency: 0.00002  dbSNP: rs1273140767
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002123728 SCV002443695 likely benign Neurofibromatosis, type 2 2024-01-28 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV002123728 SCV004818798 likely benign Neurofibromatosis, type 2 2023-12-01 criteria provided, single submitter clinical testing

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