ClinVar Miner

Submissions for variant NM_015178.3(RHOBTB2):c.1150C>T (p.Arg384Cys)

dbSNP: rs780271859
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
New York Genome Center RCV004799639 SCV001468880 uncertain significance Developmental and epileptic encephalopathy, 64 2019-08-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003106177 SCV003781982 benign not provided 2024-09-05 criteria provided, single submitter clinical testing

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