ClinVar Miner

Submissions for variant NM_000276.4(OCRL):c.235A>G (p.Asn79Asp)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002886339 SCV003246993 benign Lowe syndrome 2024-10-10 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005045034 SCV005683235 likely benign Dent disease type 2; Lowe syndrome 2024-02-23 criteria provided, single submitter clinical testing

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