ClinVar Miner

Submissions for variant NM_000545.8(HNF1A):c.1624-39C>G

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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 RCV003736451 SCV004564992 likely benign not provided 2023-06-13 criteria provided, single submitter clinical testing

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