ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.7533C>G (p.Val2511=)

dbSNP: rs760733171
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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 RCV001425464 SCV001628092 likely benign Neurofibromatosis, type 1 2020-03-17 criteria provided, single submitter clinical testing

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