ClinVar Miner

Submissions for variant NM_002900.3(RBP3):c.816C>A (p.Gly272=)

dbSNP: rs148432607
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000364801 SCV000337023 likely benign not specified 2015-12-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000880112 SCV001023183 likely benign not provided 2025-01-21 criteria provided, single submitter clinical testing
Clinical Genetics, Academic Medical Center RCV000364801 SCV001917608 benign not specified no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV000364801 SCV001969415 benign not specified no assertion criteria provided clinical testing

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