ClinVar Miner

Submissions for variant NM_001042492.3(NF1):c.1098A>G (p.Arg366=)

dbSNP: rs1597681964
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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 RCV001427475 SCV001630157 likely benign Neurofibromatosis, type 1 2018-10-06 criteria provided, single submitter clinical testing

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