ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.*1618T>C

gnomAD frequency: 0.00213  dbSNP: rs184477204
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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 RCV000326173 SCV000437797 likely benign Neurofibromatosis, type 2 2016-06-14 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV002275013 SCV002563711 likely benign not provided 2022-11-01 criteria provided, single submitter clinical testing NF2: BS1

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