ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.8004G>A (p.Leu2668=)

dbSNP: rs1597868098
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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 RCV001444959 SCV001647977 likely benign Neurofibromatosis, type 1 2018-11-11 criteria provided, single submitter clinical testing

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