ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.4332+18T>C

gnomAD frequency: 0.00001  dbSNP: rs1482009295
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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 RCV002168122 SCV002348204 likely benign Neurofibromatosis, type 1 2024-10-27 criteria provided, single submitter clinical testing

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