ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.4G>T (p.Ala2Ser) (rs1601515682)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center,Shahid Beheshti University of Medical Sciences RCV000791157 SCV000930431 uncertain significance Neurofibromatosis, type 2 2019-04-27 criteria provided, single submitter clinical testing
Genomic Research Center,Shahid Beheshti University of Medical Sciences RCV000791158 SCV000930432 uncertain significance Schwannomatosis 1 2019-04-27 criteria provided, single submitter clinical testing
Genomic Research Center,Shahid Beheshti University of Medical Sciences RCV000791159 SCV000930433 uncertain significance Meningioma, familial 2019-04-27 criteria provided, single submitter clinical testing

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