ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.*3189G>T

dbSNP: rs886057383
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000346019 SCV000437846 uncertain significance Neurofibromatosis, type 2 2016-06-14 criteria provided, single submitter clinical testing

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