ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.*3319del

dbSNP: rs372162228
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000298291 SCV000437851 uncertain significance Neurofibromatosis, type 2 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV003422327 SCV004154853 benign not provided 2022-07-01 criteria provided, single submitter clinical testing NF2: BS1, BS2

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