ClinVar Miner

Submissions for variant NC_000023.11:g.154518341C>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 RCV005242688 SCV005894344 likely benign not provided 2025-03-01 criteria provided, single submitter clinical testing G6PD: BS1

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