Variants with conflicting interpretations "uncertain significance" from Personalized Diabetes Medicine Program, University of Maryland School of Medicine and "likely pathogenic" from any submitter

Minimum review status of the submission from Personalized Diabetes Medicine Program, University of Maryland School of Medicine:		Collection method of the submission from Personalized Diabetes Medicine Program, University of Maryland School of Medicine:
Minimum review status of the other submission:		Collection method of the other submission:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 1

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HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.616T>A (p.Trp206Arg)	rs1057524898

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