ClinVar Miner

Submissions for variant NM_001348716.2(KDM6B):c.2623G>A (p.Gly875Ser)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV004722703 SCV005329700 uncertain significance not provided 2024-08-01 criteria provided, single submitter clinical testing

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