ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.465del (p.Ser156fs)

dbSNP: rs1555992948
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Human Genetics, Inc, Center for Human Genetics, Inc RCV000660132 SCV000782123 likely pathogenic Neurofibromatosis, type 2 2016-11-01 criteria provided, single submitter clinical testing

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