ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.1575-67G>A

gnomAD frequency: 0.99995  dbSNP: rs140086
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000990419 SCV001141400 benign Neurofibromatosis, type 2 2019-05-28 criteria provided, single submitter clinical testing
GeneDx RCV001672996 SCV001887703 benign not provided 2018-06-24 criteria provided, single submitter clinical testing

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