ClinVar Miner

Submissions for variant NM_015178.3(RHOBTB2):c.296+16A>G

gnomAD frequency: 0.85861  dbSNP: rs2430811
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001676509 SCV001893057 benign not provided 2019-03-25 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001796685 SCV002033603 benign Developmental and epileptic encephalopathy, 64 2021-11-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001676509 SCV002417794 benign not provided 2024-02-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001676509 SCV005268895 benign not provided criteria provided, single submitter not provided

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