ClinVar Miner

Submissions for variant NM_000342.4(SLC4A1):c.1626+7G>T

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV005234447 SCV005878402 likely benign not provided 2024-07-30 criteria provided, single submitter clinical testing

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