ClinVar Miner

Submissions for variant NC_000006.12:g.7427051ACAA[1]

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Oxford Medical Genetics Laboratories, Oxford University Hospitals NHS Foundation Trust RCV003326056 SCV003853451 uncertain significance Neonatal hemochromatosis 2023-03-23 criteria provided, single submitter clinical testing

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