ClinVar Miner

Submissions for variant NM_000545.8(HNF1A):c.713+13G>A

gnomAD frequency: 0.00004  dbSNP: rs755961371
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002096222 SCV002397866 likely benign not provided 2024-11-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494223 SCV002794767 likely benign 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 2022-01-25 criteria provided, single submitter clinical testing

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