ClinVar Miner

Submissions for variant NM_004859.4(CLTC):c.4827+1241del

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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 RCV003428357 SCV004145789 likely benign not provided 2022-11-01 criteria provided, single submitter clinical testing CLTC: BS1

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