ClinVar Miner

Submissions for variant NM_052876.4(NACC1):c.-8-7C>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 RCV003421850 SCV004137953 benign not provided 2022-03-01 criteria provided, single submitter clinical testing NACC1: BS1, BS2

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