ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.1575-6C>T

gnomAD frequency: 0.00002  dbSNP: rs1350177470
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000875101 SCV001017378 likely benign Neurofibromatosis, type 2 2025-01-30 criteria provided, single submitter clinical testing
All of Us Research Program, National Institutes of Health RCV000875101 SCV004823950 likely benign Neurofibromatosis, type 2 2023-12-01 criteria provided, single submitter clinical testing

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