ClinVar Miner

Submissions for variant NM_004859.4(CLTC):c.3905_3911del (p.Met1302fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University of Wuerzburg RCV003444028 SCV004171062 likely pathogenic Intellectual disability, autosomal dominant 56 no assertion criteria provided clinical testing

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