ClinVar Miner

Submissions for variant NM_000545.8(HNF1A):c.1401G>A (p.Pro467=)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003834418 SCV004638017 likely benign not provided 2024-05-10 criteria provided, single submitter clinical testing

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