Variants with conflicting interpretations "likely pathogenic" from Cellular and Molecular Medicine Research Institute, Urmia University of Medical Sciences and "pathogenic" from any submitter

Minimum review status of the submission from Cellular and Molecular Medicine Research Institute, Urmia University of Medical Sciences:		Collection method of the submission from Cellular and Molecular Medicine Research Institute, Urmia University of Medical Sciences:
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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000277.3(PAH):c.728G>A (p.Arg243Gln)	rs62508588	0.00001
NM_000277.3(PAH):c.1092_1094del (p.Leu365del)	rs62516096

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