ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.1062+8_1062+13del

dbSNP: rs2143874865
Minimum review status: Collection method:
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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 RCV001498722 SCV001703475 likely benign Neurofibromatosis, type 1 2020-09-23 criteria provided, single submitter clinical testing

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