ClinVar Miner

Submissions for variant NM_000276.4(OCRL):c.778C>T (p.Pro260Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005041581 SCV005683245 uncertain significance Dent disease type 2; Lowe syndrome 2023-12-26 criteria provided, single submitter clinical testing

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