ClinVar Miner

Submissions for variant NM_006565.4(CTCF):c.1697G>A (p.Arg566His)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV003985061 SCV004801344 uncertain significance Intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome 2024-02-20 criteria provided, single submitter clinical testing

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