ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.4174-15A>C

dbSNP: rs2151461679
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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 RCV002217201 SCV002362708 likely benign Neurofibromatosis, type 1 2021-06-25 criteria provided, single submitter clinical testing

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