ClinVar Miner

Submissions for variant NC_000017.11:g.31379017T>C

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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 RCV003885443 SCV004698213 likely benign not provided 2024-11-01 criteria provided, single submitter clinical testing NF1: BS1

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