ClinVar Miner

Submissions for variant NM_000458.4(HNF1B):c.831G>A (p.Gly277=)

dbSNP: rs199797518
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetic Services Laboratory, University of Chicago RCV001820517 SCV002070043 likely benign not specified 2020-01-03 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002503319 SCV002796842 likely benign Renal cysts and diabetes syndrome; Type 2 diabetes mellitus; Nonpapillary renal cell carcinoma 2021-11-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002542048 SCV003486053 likely benign not provided 2023-09-04 criteria provided, single submitter clinical testing

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