ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.480-3dup

dbSNP: rs2143706767
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002117873 SCV002406525 benign Neurofibromatosis, type 1 2023-10-13 criteria provided, single submitter clinical testing

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