ClinVar Miner

Submissions for variant NM_000545.8(HNF1A):c.1107+6T>C

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Fulgent Genetics, Fulgent Genetics RCV005012785 SCV005634494 uncertain significance Diabetes mellitus type 1; Type 1 diabetes mellitus 20; Maturity-onset diabetes of the young type 3; Type 2 diabetes mellitus; Hepatic adenomas, familial; Nonpapillary renal cell carcinoma 2024-04-14 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV003151533 SCV003839578 likely benign not specified 2022-08-29 no assertion criteria provided clinical testing

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