ClinVar Miner

Submissions for variant NM_000545.6(HNF1A):c.1502-14T>C (rs765596650)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000249865 SCV000305100 likely benign not specified criteria provided, single submitter clinical testing
Athena Diagnostics Inc RCV000249865 SCV000613601 uncertain significance not specified 2016-11-25 criteria provided, single submitter clinical testing

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