ClinVar Miner

Submissions for variant NM_000268.4(NF2):c.1737+2098A>G

gnomAD frequency: 0.00053  dbSNP: rs75296199
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003422005 SCV004154852 likely benign not provided 2023-08-01 criteria provided, single submitter clinical testing NF2: BS1
ITMI RCV000122432 SCV000083983 not provided not specified 2013-09-19 no assertion provided reference population
Knight Diagnostic Laboratories, Oregon Health and Sciences University RCV000415693 SCV000493776 uncertain significance Neurofibromatosis, type 2 2015-12-19 no assertion criteria provided clinical testing

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