ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.918T>C (p.Ala306=)

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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 RCV005169992 SCV005794813 likely benign Neurofibromatosis, type 1 2024-04-09 criteria provided, single submitter clinical testing

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