ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.4176G>T (p.Val1392=)

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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 RCV005134997 SCV005763618 likely benign Neurofibromatosis, type 1 2024-07-21 criteria provided, single submitter clinical testing

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