ClinVar Miner

Submissions for variant NM_145886.4(PIDD1):c.1302+1G>A

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MVZ Martinsried, Medicover Genetics RCV004776327 SCV005387607 likely pathogenic Intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly 2024-08-27 criteria provided, single submitter clinical testing

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