ClinVar Miner

Submissions for variant NM_000545.8(HNF1A):c.1502-19CT[2]

dbSNP: rs753496283
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics RCV004998953 SCV001880071 benign not specified 2024-07-17 criteria provided, single submitter clinical testing
GeneDx RCV001665498 SCV002504591 likely benign not provided 2020-04-06 criteria provided, single submitter clinical testing See Variant Classification Assertion Criteria.
Labcorp Genetics (formerly Invitae), Labcorp RCV001665498 SCV003470938 likely benign not provided 2024-10-03 criteria provided, single submitter clinical testing

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