ClinVar Miner

Submissions for variant NM_004715.5(CTDP1):c.314+7111G>T

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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 RCV002292971 SCV002585689 benign not provided 2022-08-01 criteria provided, single submitter clinical testing CTDP1: BS1, BS2

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