ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.1341G>A (p.Arg447=)

dbSNP: rs2066911364
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001347128 SCV001541374 likely benign Neurofibromatosis, type 2 2023-12-02 criteria provided, single submitter clinical testing
Ambry Genetics RCV002384483 SCV002694565 likely benign Hereditary cancer-predisposing syndrome 2020-07-10 criteria provided, single submitter clinical testing This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.
All of Us Research Program, National Institutes of Health RCV001347128 SCV004817403 likely benign Neurofibromatosis, type 2 2023-07-10 criteria provided, single submitter clinical testing

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