Variants with conflicting interpretations "likely pathogenic" from Genetics Laboratory, UDIAT-Centre Diagnòstic, Hospital Universitari Parc Tauli and "benign" from any submitter

Minimum review status of the submission from Genetics Laboratory, UDIAT-Centre Diagnòstic, Hospital Universitari Parc Tauli:		Collection method of the submission from Genetics Laboratory, UDIAT-Centre Diagnòstic, Hospital Universitari Parc Tauli:
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_015570.4(AUTS2):c.1717C>T (p.Pro573Ser)	rs1051952947	0.00005
NM_017613.4(DONSON):c.1466A>C (p.Lys489Thr)	rs146664036

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