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

Minimum review status:		Collection method:
Minimum conflict level:
		ClinVar version:

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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