ClinVar Miner

Submissions for variant NM_002072.5(GNAQ):c.736-18dup

dbSNP: rs5898555
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000947185 SCV001093356 benign not provided 2019-12-31 criteria provided, single submitter clinical testing
GeneDx RCV000947185 SCV001855404 benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV000947185 SCV001798051 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001701369 SCV001921385 benign not specified no assertion criteria provided clinical testing

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