ClinVar Miner

Submissions for variant NM_000268.3(NF2):c.107A>G (p.Asn36Ser) (rs372279458)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000564583 SCV000674122 uncertain significance Hereditary cancer-predisposing syndrome 2017-10-23 criteria provided, single submitter clinical testing Lines of evidence used in support of classification: Insufficient evidence
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000733228 SCV000861268 uncertain significance not provided 2018-05-29 criteria provided, single submitter clinical testing
ITMI RCV000121642 SCV000085840 not provided not specified 2013-09-19 no assertion provided reference population
Invitae RCV000228532 SCV000284538 benign Neurofibromatosis, type 2 2017-12-18 criteria provided, single submitter clinical testing

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