ClinVar Miner

Submissions for variant NM_002717.4(PPP2R2A):c.82+57A>G

dbSNP: rs372615585
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
National Health Laboratory Service, Universitas Academic Hospital and University of the Free State RCV002226376 SCV002505259 likely benign Hereditary breast ovarian cancer syndrome 2022-04-19 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004707799 SCV005222875 likely benign not provided criteria provided, single submitter not provided

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