ClinVar Miner

Submissions for variant NM_000276.4(OCRL):c.200-11dup

dbSNP: rs765652296
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002120801 SCV002440824 benign Lowe syndrome 2024-01-13 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500187 SCV002808612 likely benign Dent disease type 2; Lowe syndrome 2022-04-11 criteria provided, single submitter clinical testing

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